chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1241510092241510092G6GENIChomozygous127497415
1241510095241510095T6GENIChomozygous127497416
1241510097241510097G6GENIChomozygous127497417
1241510184241510184T3GENIChomozygous127497419
1241510194241510194C3GENIChomozygous127497420
1241510231241510232AG12GENIChomozygous120476557
1241510232241510233GA12GENIChomozygous120476558
1241510266241510266G13GENIChomozygous127497421
1241510274241510275C12GENIChomozygous127497422
1241510280241510280T13GENIChomozygous127497423
1241510293241510293G13GENIChomozygous127497424
1241510316241510316G11GENIChomozygous127497425
1241510317241510317T11GENIChomozygous127497426
1241510328241510328C11GENIChomozygous127497427
1241515200241515200G5GENIChomozygous127497428
1241529610241529642GACACAAAAAATAGTTGTCATCATAAACAAAG14GENIChomozygous127497429
1241531764241531765G8GENIChomozygous127497430
1241531791241531792C6GENIChomozygous127497431
1241531826241531826C2GENIChomozygous127497432
1241531828241531829GC2GENIChomozygous121201882
1241538494241538495GA15GENIChomozygous108591068
1241538679241538680C18GENIChomozygous127497433
1241539220241539221AG6GENICheterozygous121201886
1241539224241539225AG6GENICheterozygous121201888
1241540076241540077GA3GENIChomozygous127583165
1241539246241539247AG9GENICpossibly homozygous129861511
1241539951241539952GA4GENIChomozygous127583162
1241539952241539953CT4GENIChomozygous127583163
1241539986241539987GA4GENIChomozygous127583164