chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116168084116168085AG18GENIChomozygous69062500
7116168099116168100CT17GENIChomozygous69062503
7116168608116168609CT43GENIChomozygous69062506
7116169194116169195AG41GENIChomozygous69062509
7116169236116169237TC36GENIChomozygous69062512
7116169279116169280AG32GENIChomozygous69062514
7116170073116170074TC29GENIChomozygous69062517
7116170858116170859TC28GENIChomozygous69062520
7116171164116171165TG52GENIChomozygous69062522
7116171392116171393AG26GENIChomozygous69062525
7116171504116171505AG23GENIChomozygous69062528
7116171554116171555CT25GENIChomozygous69062530
7116172202116172203CT27GENIChomozygous69062533
7116173059116173060TC32GENIChomozygous69062539
7116173127116173128TC38GENIChomozygous69062542
7116173300116173301CT25GENIChomozygous69062544
7116173832116173833AC25GENIChomozygous69062560
7116173841116173842AG23GENIChomozygous69062562
7116176354116176355TC28GENIChomozygous69062568
7116177562116177563AC25GENIChomozygous69062571
7116177611116177612GA36GENIChomozygous69062574
7116177649116177650TG38GENIChomozygous69062577
7116177823116177824TC27GENIChomozygous69062579
7116178197116178198GC26GENIChomozygous69062582
7116178934116178935CT16GENIChomozygous69062585
7116179620116179621TA17GENIChomozygous69062588
7116179858116179859GA18GENIChomozygous69062590
7116181985116181986TA32GENIChomozygous69062593
7116182697116182698AG25GENIChomozygous69062596
7116189683116189684CT64GENICheterozygous69062602
7116189722116189723AC25GENICpossibly homozygous69062605
7116190066116190067AG30GENIChomozygous69062608
7116190068116190069CT29GENIChomozygous69062611
7116190295116190296GT28GENIChomozygous69062614