Table 2

Four ROH significantly associated with BCP-ALL risk (P < .01)

ROHChromosomeStart, bpEnd, bpLength, bpNo. of SNPsNo. (%) of casesNo. (%) of controlsχ2P
ROH261 10p11.21-10q11.21 36 774 789 44 190 246 7 415 457 317 26 (3.4) 140 (5.9) 9.58 < .002 
ROH15 1p31.1-1p31.1 70 726 887 76 563 751 5 836 864 463 27 (3.2) 137 (5.8) 8.04 < .005 
ROH380 19p13.2-19p13.13 11 145 302 12 633 165 1 487 863 115 18 (2.2) 22 (0.9) 7.69 < .006 
ROH388 20q11.1-20q11.23 28 121 437 35 496 979 7 375 542 401 67 (8.1) 270 (11.4) 7.14 > .007 
ROHChromosomeStart, bpEnd, bpLength, bpNo. of SNPsNo. (%) of casesNo. (%) of controlsχ2P
ROH261 10p11.21-10q11.21 36 774 789 44 190 246 7 415 457 317 26 (3.4) 140 (5.9) 9.58 < .002 
ROH15 1p31.1-1p31.1 70 726 887 76 563 751 5 836 864 463 27 (3.2) 137 (5.8) 8.04 < .005 
ROH380 19p13.2-19p13.13 11 145 302 12 633 165 1 487 863 115 18 (2.2) 22 (0.9) 7.69 < .006 
ROH388 20q11.1-20q11.23 28 121 437 35 496 979 7 375 542 401 67 (8.1) 270 (11.4) 7.14 > .007 

ROH indicates regions of homozygosity; BCP-ALL, B-cell precursor acute lymphoblastic leukemia; and SNP, single nucleotide polymorphism.

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