<p>P values are the results of two-tailed Fisher's Exact tests comparing control with either BCP-ALL or T-ALL frequency; bold format indicates uncorrected P<0.05. *P withstands Benjamini and Hochberg FDR correction for 14 haplotypes (α = 0.0036). <i>HLA-DPB1</i> alleles predicted by PHASE to be carried on each Block 4 haplotype are also shown (percentages in brackets indicate the proportion of each <i>DPB1</i> allele predicted to be carried on the haplotype.</p
<p><i>TNF</i> blocks (<i>TNF_1– TNF_9</i>) and their frequencies (>1.0%).<i>HLA-DRB1</i> Haplotypes ...
<p>Note: Haplotype 1 includes the risk alleles of rs75024165 *T and rs34379100 *C (<i>P<0.01</i>).</...
<p>Colors indicate different deviations from the null hypothesis; thus, black represents a frequency...
<p>P values are the results of two-tailed Fisher's Exact tests comparing control with either BCP-ALL...
<p>*P values were calculated by permutation testing (1000 permutations) within PHASE. Bold indicates...
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
a<p>Listed are only the top 5% of all the HLA-A-B-DRB1 haplotypes with significant uncorrected P-val...
<p>Significant p-values are in italic bold. Common Haplotypes are shown, if frequency more than 2.5%...
<p>The haplotypes shown occurred with a frequency of ≥10% in the case-control population.</p>a<p><i>...
<p>Note: <i>p</i>, unadjusted <i>p</i> values,* <i>p</i><0.05;</p><p><i>p′</i>, adjusted <i>p</i> va...
<p>MHF: minor haplotype frequency; H1, H2, H3, H4 represented haplotype1, haplotype2, haplotype3, ha...
<p>*nominal significance level: P<0.05; Bonferroni correction for significance was calculated as P<0...
<p>Comparison of genotype and allele frequencies in the control subjects of our study and those from...
<p>The magenta line represents the average of all haplotypes at a given Hamming distance. Also plott...
<p>The -log<sub>10</sub> (p-values) for each SNP (y-axis) are plotted against their chromosomal posi...
<p><i>TNF</i> blocks (<i>TNF_1– TNF_9</i>) and their frequencies (>1.0%).<i>HLA-DRB1</i> Haplotypes ...
<p>Note: Haplotype 1 includes the risk alleles of rs75024165 *T and rs34379100 *C (<i>P<0.01</i>).</...
<p>Colors indicate different deviations from the null hypothesis; thus, black represents a frequency...
<p>P values are the results of two-tailed Fisher's Exact tests comparing control with either BCP-ALL...
<p>*P values were calculated by permutation testing (1000 permutations) within PHASE. Bold indicates...
a<p>Frequencies are shown in parentheses.</p>b<p>Significant <i>P</i> values (<0.05) are in bold.</p...
a<p>Listed are only the top 5% of all the HLA-A-B-DRB1 haplotypes with significant uncorrected P-val...
<p>Significant p-values are in italic bold. Common Haplotypes are shown, if frequency more than 2.5%...
<p>The haplotypes shown occurred with a frequency of ≥10% in the case-control population.</p>a<p><i>...
<p>Note: <i>p</i>, unadjusted <i>p</i> values,* <i>p</i><0.05;</p><p><i>p′</i>, adjusted <i>p</i> va...
<p>MHF: minor haplotype frequency; H1, H2, H3, H4 represented haplotype1, haplotype2, haplotype3, ha...
<p>*nominal significance level: P<0.05; Bonferroni correction for significance was calculated as P<0...
<p>Comparison of genotype and allele frequencies in the control subjects of our study and those from...
<p>The magenta line represents the average of all haplotypes at a given Hamming distance. Also plott...
<p>The -log<sub>10</sub> (p-values) for each SNP (y-axis) are plotted against their chromosomal posi...
<p><i>TNF</i> blocks (<i>TNF_1– TNF_9</i>) and their frequencies (>1.0%).<i>HLA-DRB1</i> Haplotypes ...
<p>Note: Haplotype 1 includes the risk alleles of rs75024165 *T and rs34379100 *C (<i>P<0.01</i>).</...
<p>Colors indicate different deviations from the null hypothesis; thus, black represents a frequency...