chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157704713157704714TC11GENIChomozygous60909142
1157704779157704780CT22GENIChomozygous61544465
1157704963157704964TG14GENICpossibly homozygous61544466
1157705139157705140TC21GENIChomozygous61544467
1157705257157705258TA12GENICpossibly homozygous61544468
1157705336157705337CT1GENIChomozygous61544469
1157705337157705338CT1GENIChomozygous61544470
1157705749157705750CT4GENIChomozygous61544471
1157705933157705934CA6GENIChomozygous61544472
1157706114157706115CT22GENIChomozygous61544473
1157706222157706223GT21GENIChomozygous61544474
1157707321157707322AG8GENIChomozygous61544479
1157707339157707340TG11GENIChomozygous61544480
1157707893157707894AC11GENIChomozygous61544481
1157708142157708143CT9GENIChomozygous61544482
1157708157157708158A-6GENIChomozygous61544483
1157708169157708170GGAA3GENIChomozygous61544484
1157708392157708393AG19GENIChomozygous61544485
1157708501157708502GGAC1GENIChomozygous62555092
1157708632157708633GC17GENIChomozygous60909148