chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116507189765071898TTC20INTERGENIChomozygous50802471
116507371365073714A-21INTERGENICheterozygous50802473
116508839965088400G-37INTERGENICheterozygous50802475
116510527665105277AG39INTERGENICheterozygous50802477
116512097465120975AG36INTERGENICheterozygous50802479
116512126565121266TC37INTERGENICheterozygous50802481
116512131765121318GC42INTERGENICheterozygous50802483
116513245665132457A-6INTERGENICheterozygous50802485
116513246365132464GA9INTERGENICheterozygous50802487
116513247065132471AG14INTERGENICheterozygous50802489
116513251565132516T-23INTERGENIChomozygous50802491
116515235565152356AG16INTERGENIChomozygous50802493
116515238565152386AG3INTERGENIChomozygous50802495
116515240265152403CT3INTERGENIChomozygous50802497
116515243565152436TC6INTERGENICheterozygous50802499
116515539365155394A-38INTERGENICheterozygous50802501
116515547565155476AG130INTERGENICheterozygous50802503
116517568465175685CCAATA16INTERGENICheterozygous50802505
116518037065180371T-21INTERGENICheterozygous50802507
116518038765180388CT33INTERGENICheterozygous50802509
116518073065180731GT17INTERGENIChomozygous50802510
116518073465180735TTG13INTERGENIChomozygous50802512
116518076165180762GGT2INTERGENIChomozygous50802514
116518098965180990G-14INTERGENIChomozygous50802516
116518882265188823CCCG22INTERGENICheterozygous50802518
116518882265188823CCAG22INTERGENICheterozygous50802520
116520906365209064AG62GENIChomozygous50802522