chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116168084116168085AG10GENIChomozygous69062500
7116168099116168100CT10GENIChomozygous69062503
7116168608116168609CT27GENIChomozygous69062506
7116169194116169195AG22GENIChomozygous69062509
7116169236116169237TC20GENIChomozygous69062512
7116169279116169280AG25GENIChomozygous69062514
7116170073116170074TC19GENICpossibly homozygous69062517
7116170858116170859TC23GENIChomozygous69062520
7116171164116171165TG20GENIChomozygous69062522
7116171392116171393AG13GENIChomozygous69062525
7116171504116171505AG17GENIChomozygous69062528
7116171554116171555CT21GENIChomozygous69062530
7116172202116172203CT15GENIChomozygous69062533
7116173059116173060TC15GENIChomozygous69062539
7116173127116173128TC25GENIChomozygous69062542
7116173300116173301CT14GENIChomozygous69062544
7116173832116173833AC12GENIChomozygous69062560
7116173841116173842AG11GENIChomozygous69062562
7116176354116176355TC23GENIChomozygous69062568
7116177562116177563AC19GENIChomozygous69062571
7116177611116177612GA24GENIChomozygous69062574
7116177649116177650TG26GENIChomozygous69062577
7116177823116177824TC15GENIChomozygous69062579
7116178197116178198GC23GENIChomozygous69062582
7116178934116178935CT12GENIChomozygous69062585
7116179620116179621TA10GENIChomozygous69062588
7116179858116179859GA19GENIChomozygous69062590
7116181985116181986TA28GENIChomozygous69062593
7116182697116182698AG14GENIChomozygous69062596
7116189683116189684CT31GENICheterozygous69062602
7116190295116190296GT20GENIChomozygous69062614
7116189722116189723AC20GENICpossibly homozygous69062605
7116190066116190067AG25GENIChomozygous69062608
7116190068116190069CT24GENIChomozygous69062611