chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241510092241510092G17GENIChomozygous127497415
1241510095241510095T16GENIChomozygous127497416
1241510097241510097G14GENIChomozygous127497417
1241510156241510156A10GENIChomozygous127497418
1241510184241510184T20GENIChomozygous127497419
1241510194241510194C22GENIChomozygous127497420
1241510231241510232AG34GENIChomozygous120476557
1241510232241510233GA34GENIChomozygous120476558
1241510266241510266G37GENIChomozygous127497421
1241510274241510275C38GENIChomozygous127497422
1241510280241510280T40GENIChomozygous127497423
1241510293241510293G44GENIChomozygous127497424
1241510316241510316G50GENIChomozygous127497425
1241510317241510317T50GENIChomozygous127497426
1241510328241510328C50GENIChomozygous127497427
1241515200241515200G11GENIChomozygous127497428
1241529610241529642GACACAAAAAATAGTTGTCATCATAAACAAAG22GENIChomozygous127497429
1241531764241531765G21GENIChomozygous127497430
1241531791241531792C15GENIChomozygous127497431
1241531826241531826C9GENIChomozygous127497432
1241531828241531829GC9GENIChomozygous121201882