chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116168084116168085AG50GENIChomozygous69062500
7116170073116170074TC33GENIChomozygous69062517
7116171164116171165TG37GENIChomozygous69062522
7116171504116171505AG31GENIChomozygous69062528
7116171554116171555CT27GENIChomozygous69062530
7116172202116172203CT40GENICpossibly homozygous69062533
7116173059116173060TC23GENIChomozygous69062539
7116173127116173128TC34GENIChomozygous69062542
7116173300116173301CT36GENIChomozygous69062544
7116173415116173416CA14GENICheterozygous69062550
7116173425116173426CT16GENICheterozygous69062554
7116173430116173431TC11GENIChomozygous69062557
7116173832116173833AC19GENIChomozygous69062560
7116173841116173842AG16GENIChomozygous69062562
7116174658116174659CT8GENIChomozygous69062565
7116176354116176355TC30GENIChomozygous69062568
7116177562116177563AC35GENIChomozygous69062571
7116177649116177650TG28GENICpossibly homozygous69062577
7116178934116178935CT29GENIChomozygous69062585
7116179319116179320GA29GENIChomozygous70240684
7116170769116170770CG20GENIChomozygous70240669
7116172141116172142GA33GENIChomozygous70240672
7116173271116173272CT38GENIChomozygous70240675
7116174402116174403CT30GENIChomozygous70240678
7116179253116179254GA25GENIChomozygous70240681
7116173423116173424TC14GENICheterozygous71511234
7116173430116173431TA5GENIChomozygous71511238
7116179863116179864GA29GENIChomozygous70240687
7116179991116179992CT27GENIChomozygous70240690
7116181985116181986TA29GENIChomozygous69062593
7116182697116182698AG35GENIChomozygous69062596
7116182863116182864CT39GENIChomozygous70240693
7116189508116189509TC25GENIChomozygous70240696
7116189515116189516TC24GENIChomozygous70240699
7116189677116189678TC16GENICheterozygous69062599
7116189683116189684CT17GENICheterozygous69062602
7116190066116190067AG39GENIChomozygous69062608
7116190068116190069CT39GENIChomozygous69062611
7116180519116180520TG9GENICheterozygous71588128
7116182983116182984TA7GENIChomozygous71588131
7116189484116189485TC17GENIChomozygous70612681