chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103572866135728662GA15GENIChomozygous51847463
103573000935730010GGTGTC9GENIChomozygous51409562
103573137435731375TG7GENIChomozygous51409569
103573183335731834GGA18GENIChomozygous51409571
103573326435733265CG12GENIChomozygous51409580
103573378635733787G-11GENIChomozygous51409583
103573384735733848TC14GENIChomozygous51409585
103573387035733871GA11GENIChomozygous51409587
103573389635733897AG10GENIChomozygous51409588
103573394335733944CT13GENIChomozygous51409590
103573395535733956GA16GENIChomozygous51409592
103573396735733968TC17GENIChomozygous51409594
103573397535733976GA16GENIChomozygous51409596
103573398235733983AG16GENIChomozygous51409598
103573414435734145GT7GENIChomozygous51409602
103573434335734344TC11GENIChomozygous51409604
103573452335734524TC14GENIChomozygous51409606
103573465835734659TA11GENIChomozygous51409610
103573477335734774TA10GENIChomozygous51409612
103573501635735017CT18GENIChomozygous51847484
103573532135735322AG18GENIChomozygous51847487
103573532935735330TA17GENIChomozygous51847490
103573533735735338TA18GENIChomozygous51409614
103573543735735438TG16GENIChomozygous51847493
103573552535735526GA7GENIChomozygous51847496
103573584035735841GT9GENIChomozygous51847499
103573628235736283TC10GENIChomozygous51409624
103573722735737228CCG19GENIChomozygous51409626
103573761635737617TG15GENIChomozygous51409628
103573773535737736AG10GENIChomozygous51847502
103573850035738501CT14GENIChomozygous51847505
103573972635739727CA12GENIChomozygous51847510
103573991535739916TC7GENIChomozygous51409644
103574084135740842AG10GENIChomozygous51409646
103574185735741858TA13GENICheterozygous52316216