chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241510092241510092G1GENIChomozygous127497415
1241510095241510095T1GENIChomozygous127497416
1241510097241510097G1GENIChomozygous127497417
1241510156241510156A5GENIChomozygous127497418
1241510184241510184T7GENIChomozygous127497419
1241510194241510194C7GENIChomozygous127497420
1241510266241510266G15GENIChomozygous127497421
1241510274241510275C15GENIChomozygous127497422
1241510280241510280T14GENIChomozygous127497423
1241510293241510293G14GENIChomozygous127497424
1241510316241510316G14GENIChomozygous127497425
1241510317241510317T15GENIChomozygous127497426
1241510328241510328C15GENIChomozygous127497427
1241515200241515200G8GENIChomozygous127497428
1241529610241529642GACACAAAAAATAGTTGTCATCATAAACAAAG15GENIChomozygous127497429
1241531764241531765G6GENIChomozygous127497430
1241531791241531792C5GENIChomozygous127497431
1241531826241531826C2GENIChomozygous127497432
1241531828241531829GC2GENIChomozygous121201882
1241510231241510232AG11GENIChomozygous120476557
1241510232241510233GA11GENIChomozygous120476558