chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1825064932506494TC21GENIChomozygous64005397
1825066042506605AG26GENIChomozygous64005399
1825099672509968AG36GENIChomozygous64005409
1825203332520334AG39GENIChomozygous64005427
1825206292520630AT27GENIChomozygous64126019
1825208292520830TC34GENIChomozygous64126020
1825208502520851CT31GENIChomozygous64005429
1825211672521168GA26GENIChomozygous64126021
1825213252521326AT27GENIChomozygous64126022
1825127002512701CT35GENIChomozygous84635520
1825171192517120TA30GENIChomozygous84635521
1825219602521961TC20GENICpossibly homozygous64005433
1825228532522854TC31GENIChomozygous64126023
1825246042524605TC32GENIChomozygous64005441
1825252192525220CT35GENICpossibly homozygous64005443
1825252602525261TA21GENIChomozygous64126024
1825260082526009CT34GENIChomozygous64005445
1825260282526029AG39GENIChomozygous64005447
1825267692526770AG25GENIChomozygous64005451
1825281852528186AT25GENIChomozygous64005457
1825284432528444AG28GENIChomozygous64005461
1825285962528597TC24GENIChomozygous64126025
1825285992528600AG26GENIChomozygous64005463
1825286462528647TC23GENIChomozygous64085970
1825286502528651CT25GENIChomozygous64126026
1825287092528710TC41GENIChomozygous64005465
1825334802533481AG31GENIChomozygous84635522