chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187114784187114785TC54GENIChomozygous110166930
2187114899187114900TA37GENIChomozygous111146520
2187114917187114918AG29GENIChomozygous110166931
2187115561187115562AG69GENICpossibly homozygous110166932
2187116861187116862AG67GENIChomozygous110166933
2187118331187118332CT61GENIChomozygous120377903
2187118926187118927AG71GENIChomozygous111146522
2187119021187119022CT51GENIChomozygous120377904
2187119229187119230TC70GENIChomozygous111146523
2187120234187120235GA51GENIChomozygous120377905
2187120264187120265CT46GENIChomozygous111146524
2187120758187120759GT17GENIChomozygous120377906
2187120951187120952CG77GENIChomozygous120377907
2187121209187121210AG85GENIChomozygous110166937
2187121900187121901AG76GENIChomozygous110166938
2187121949187121950GA89GENIChomozygous111146526
2187122491187122492AG38GENIChomozygous111146527
2187122572187122573TC77GENIChomozygous111146528
2187123733187123734GA41GENIChomozygous120377908
2187123766187123767TC36GENIChomozygous120377909
2187124587187124588AG58GENIChomozygous120377910
2187125276187125277GT56GENIChomozygous120377911
2187127136187127137AG41GENIChomozygous120377912
2187127743187127744CT77GENIChomozygous120377913
2187128015187128016AG40GENIChomozygous120377914
2187128397187128398AG37GENIChomozygous120377915
2187128673187128674AG28GENIChomozygous120377916
2187128801187128802TC59GENIChomozygous120377917
2187128947187128948CT51GENIChomozygous120377918
2187130307187130308TG41GENIChomozygous120377919
2187130331187130332GA32GENIChomozygous110166948
2187130775187130776CT31GENIChomozygous120377920
2187131905187131906GA83GENIChomozygous120377921
2187132171187132172AG34GENIChomozygous120377922
2187132808187132809GA68GENIChomozygous120377923
2187133082187133083CT80GENIChomozygous120377924
2187133512187133513GC37GENIChomozygous120377925
2187133753187133754CT24GENIChomozygous120393688