chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38023305780233058GA30GENIChomozygous57487286
38023306480233065CA31GENIChomozygous57487288
38023314080233141AG14GENIChomozygous57487290
38023325580233256GA27GENIChomozygous57487292
38023326680233267GA24GENIChomozygous57487294
38023328280233283TC21GENIChomozygous57487296
38023332180233322CT25GENIChomozygous57487299
38023336880233369CT30GENICpossibly homozygous57487301
38023349880233499GA19GENIChomozygous57487303
38023352280233523GA19GENIChomozygous57487305
38023363880233639CT33GENICpossibly homozygous57487307
38023364180233642TA32GENICpossibly homozygous57487309
38023364280233643CA32GENICpossibly homozygous57487311
38023365180233652AG33GENIChomozygous57487313
38023377480233775AG17GENICpossibly homozygous57487315
38023386480233865AG17GENIChomozygous57487317
38023386780233868GC17GENIChomozygous57487319
38023387880233879CT17GENIChomozygous57487321
38023388080233881GA17GENIChomozygous57487323
38023389480233895GA22GENIChomozygous57487325
38023395080233951TC24GENIChomozygous57487327