chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2200397131200397132GA27GENIChomozygous110204313
2200398084200398085AC44GENIChomozygous110204314
2200398407200398408GT28GENIChomozygous110204315
2200398441200398442CA32GENIChomozygous110204316
2200400188200400189GA22GENIChomozygous110204317
2200400914200400915GA34GENIChomozygous110204318
2200401038200401039CT28GENIChomozygous110204319
2200401428200401429AG47GENIChomozygous110204320
2200402848200402849TC20GENIChomozygous110204321
2200403180200403181CT14GENIChomozygous110204322
2200403687200403688TC32GENIChomozygous110204323
2200403715200403716AG35GENIChomozygous110204324
2200404030200404031TG27GENIChomozygous110204325
2200404048200404049CT26GENIChomozygous110204326
2200404839200404840GA20GENIChomozygous110204327
2200404851200404852GA20GENIChomozygous110204328
2200404869200404870AG17GENIChomozygous110204329
2200405326200405327AT24GENIChomozygous110204330
2200405675200405676CG21GENIChomozygous110204331
2200405978200405979GT33GENIChomozygous110204332
2200407465200407466GT53GENICpossibly homozygous110204333
2200407783200407784TG13GENIChomozygous110204334
2200408195200408196CT35GENIChomozygous110204335
2200408385200408386TC30GENIChomozygous110204336
2200408591200408592TC14GENIChomozygous110204337
2200408960200408961GA49GENICpossibly homozygous110204338
2200409534200409535AG20GENIChomozygous110204339
2200409641200409642AG21GENIChomozygous110204340