chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2104055961104055962CT7GENICheterozygous125628522
2104055967104055968TA8GENICheterozygous125628523
2104059814104059815CT5GENICheterozygous125628524
2104119986104119987TA10GENIChomozygous125577606
2104120187104120188TA10GENIChomozygous125577608
2104120345104120346TC4GENIChomozygous125577610
2104120358104120359CG4GENIChomozygous125577611
2104120431104120432CA15GENIChomozygous125577612
2104120445104120446TA9GENIChomozygous125577613
2104120458104120459TA6GENIChomozygous125577614
2104120500104120501AT9GENIChomozygous125577615
2104120509104120510CG12GENIChomozygous125577616
2104120518104120519AT13GENIChomozygous125577617
2104122275104122276AG5GENIChomozygous109958287
2104129370104129371CT4GENICheterozygous125628525
2104130095104130096CA22GENIChomozygous125577618
2104131090104131091GA7GENIChomozygous125577619