chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241510092241510092G14GENIChomozygous127497415
1241510095241510095T13GENIChomozygous127497416
1241510097241510097G11GENIChomozygous127497417
1241510156241510156A7GENIChomozygous127497418
1241510184241510184T9GENIChomozygous127497419
1241510194241510194C10GENIChomozygous127497420
1241510231241510232AG28GENIChomozygous120476557
1241510232241510233GA29GENIChomozygous120476558
1241510266241510266G32GENIChomozygous127497421
1241510274241510275C35GENIChomozygous127497422
1241510280241510280T35GENIChomozygous127497423
1241510293241510293G33GENIChomozygous127497424
1241510316241510316G31GENIChomozygous127497425
1241510317241510317T33GENIChomozygous127497426
1241510328241510328C35GENIChomozygous127497427
1241515200241515200G10GENIChomozygous127497428
1241529610241529642GACACAAAAAATAGTTGTCATCATAAACAAAG32GENIChomozygous127497429
1241531828241531829GC9GENIChomozygous121201882
1241531764241531765G20GENIChomozygous127497430
1241531791241531792C16GENIChomozygous127497431
1241531826241531826C9GENIChomozygous127497432