chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7116170073116170074TC12GENIChomozygous69062517
7116170769116170770CG17GENIChomozygous70240669
7116171164116171165TG20GENIChomozygous69062522
7116171504116171505AG20GENICpossibly homozygous69062528
7116171554116171555CT23GENIChomozygous69062530
7116172141116172142GA29GENIChomozygous70240672
7116172202116172203CT32GENIChomozygous69062533
7116173059116173060TC17GENIChomozygous69062539
7116173127116173128TC18GENIChomozygous69062542
7116173271116173272CT10GENIChomozygous70240675
7116173300116173301CT17GENIChomozygous69062544
7116173832116173833AC6GENIChomozygous69062560
7116173841116173842AG9GENIChomozygous69062562
7116174402116174403CT5GENIChomozygous70240678
7116174658116174659CT14GENIChomozygous69062565
7116176354116176355TC20GENIChomozygous69062568
7116177562116177563AC17GENIChomozygous69062571
7116177649116177650TG16GENIChomozygous69062577
7116178934116178935CT16GENIChomozygous69062585
7116179253116179254GA15GENIChomozygous70240681
7116179319116179320GA18GENIChomozygous70240684
7116179863116179864GA8GENIChomozygous70240687
7116179991116179992CT18GENIChomozygous70240690
7116181985116181986TA25GENIChomozygous69062593
7116182697116182698AG15GENIChomozygous69062596
7116182863116182864CT21GENIChomozygous70240693
7116189515116189516TC7GENIChomozygous70240699
7116189677116189678TC3GENIChomozygous69062599
7116190066116190067AG10GENIChomozygous69062608
7116190068116190069CT11GENIChomozygous69062611
7116171081116171082GA4GENIChomozygous70800962
7116189602116189602CACT19GENICheterozygous70800965
7116189484116189485TC15GENIChomozygous70612681