chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116168084116168085AG17GENIChomozygous69062500
7116168099116168100CT20GENIChomozygous69062503
7116168608116168609CT16GENIChomozygous69062506
7116169194116169195AG18GENIChomozygous69062509
7116169236116169237TC21GENIChomozygous69062512
7116169279116169280AG17GENIChomozygous69062514
7116170073116170074TC18GENIChomozygous69062517
7116170858116170859TC21GENIChomozygous69062520
7116171164116171165TG22GENIChomozygous69062522
7116171392116171393AG21GENIChomozygous69062525
7116171504116171505AG18GENIChomozygous69062528
7116171554116171555CT31GENIChomozygous69062530
7116172202116172203CT20GENIChomozygous69062533
7116173059116173060TC19GENIChomozygous69062539
7116173127116173128TC16GENIChomozygous69062542
7116173300116173301CT9GENIChomozygous69062544
7116173832116173833AC22GENIChomozygous69062560
7116173841116173842AG21GENIChomozygous69062562
7116176354116176355TC30GENIChomozygous69062568
7116177562116177563AC19GENIChomozygous69062571
7116177611116177612GA17GENIChomozygous69062574
7116177649116177650TG17GENIChomozygous69062577
7116177823116177824TC17GENIChomozygous69062579
7116178197116178198GC26GENIChomozygous69062582
7116178934116178935CT17GENIChomozygous69062585
7116179620116179621TA19GENIChomozygous69062588
7116179858116179859GA21GENIChomozygous69062590
7116181985116181986TA26GENIChomozygous69062593
7116182697116182698AG18GENIChomozygous69062596
7116189683116189684CT29GENICheterozygous69062602
7116189722116189723AC13GENICpossibly homozygous69062605
7116190066116190067AG35GENIChomozygous69062608
7116190068116190069CT34GENIChomozygous69062611
7116190295116190296GT17GENIChomozygous69062614