chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214375955214375956TC27GENIChomozygous108532379
1214377502214377503TC27GENIChomozygous108532380
1214377599214377600CA31GENIChomozygous108532381
1214377709214377710TG24GENICpossibly homozygous108532382
1214377935214377936CA28GENIChomozygous108532383
1214378309214378310CT48GENIChomozygous108532384
1214378647214378648GA32GENIChomozygous108532386
1214379430214379431AG28GENIChomozygous108532387
1214379707214379708GC24GENIChomozygous108532388
1214379953214379954AG40GENIChomozygous108532389
1214381179214381180CT19GENIChomozygous108532392
1214382436214382437GA42GENIChomozygous108532398
1214382582214382583AC27GENIChomozygous108532399
1214382788214382789TC38GENIChomozygous108532400
1214384631214384632GA35GENIChomozygous108532401