chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2244040474244040475CA3GENICheterozygous120433692
2244040902244040903CT13GENIChomozygous110350591
2244042585244042586CT4GENIChomozygous110350600
2244042949244042950TC27GENIChomozygous110350602
2244044150244044151TC8GENIChomozygous110350606
2244044776244044777TC21GENIChomozygous110350608
2244045755244045756GA17GENIChomozygous110350610
2244046036244046037TC20GENIChomozygous110350612
2244046217244046218GT14GENIChomozygous110350614
2244046511244046512AT22GENIChomozygous110350616
2244046525244046526GC20GENIChomozygous110350618
2244047064244047065CT25GENIChomozygous110350620
2244047123244047124GT18GENIChomozygous110350622
2244047540244047541GC20GENIChomozygous110350624
2244047738244047739CT24GENIChomozygous110350626
2244047847244047848GA32GENIChomozygous110350628
2244048097244048098TC17GENIChomozygous110350630
2244048640244048641TC20GENIChomozygous110350632
2244048645244048646TC21GENIChomozygous110350633
2244049002244049003GA21GENIChomozygous110350635
2244049245244049246CG21GENIChomozygous110350637
2244049413244049414CT28GENIChomozygous110350639
2244049722244049723GA27GENIChomozygous110350641
2244049727244049728TC30GENIChomozygous110350643
2244049914244049915CT24GENIChomozygous110350645
2244050459244050460AG27GENIChomozygous110350647
2244051081244051082GA23GENIChomozygous110350649
2244051272244051273GC32GENIChomozygous110350651
2244051354244051355AG20GENIChomozygous110350653
2244051413244051414AG18GENIChomozygous110350655
2244051685244051686GA25GENIChomozygous110350657
2244051968244051969TC16GENIChomozygous110350659
2244052107244052108CT25GENIChomozygous110350661
2244052186244052187TC28GENIChomozygous110350663
2244052674244052675GA21GENIChomozygous110350665
2244053205244053206AG21GENIChomozygous110350667
2244053301244053302AC26GENIChomozygous120180162
2244055724244055725CT19GENIChomozygous110350669
2244056383244056384AG16GENIChomozygous110350671
2244056684244056685CG23GENIChomozygous110350673