chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12945115945116TC7GENIChomozygous126217490
12946156946157CG12GENIChomozygous126161116
12946197946198CT13GENIChomozygous126217493
12946206946207GC12GENIChomozygous126161117
12946226946227TG12GENIChomozygous126217495
12946302946303GA20GENIChomozygous126161118
12946371946372GT26GENIChomozygous126217497
12955626955627TC28GENIChomozygous126161119
12957662957663AG18GENIChomozygous126217505
12958579958580AG15GENIChomozygous126161121
12961972961973AG21GENIChomozygous126217508
12962403962404CA20GENIChomozygous126207994
12963159963160AG21GENIChomozygous126217510
12965095965096CT13GENIChomozygous126217512
12965632965633GT16GENIChomozygous126217514
12965740965741GA29GENIChomozygous126217516
12965933965934AG15GENIChomozygous126217519
12965997965998AG17GENIChomozygous126217521
12967097967098AG17GENIChomozygous126217523
12969000969001AG21GENIChomozygous126217525
12970736970737AC13GENIChomozygous126208002
12971497971498CA13GENIChomozygous126161125
12971621971622CT22GENIChomozygous126217528
12971711971712CG27GENIChomozygous126161126
12972555972556TC21GENICheterozygous126217530
12976611976612GA17GENIChomozygous126208004
12976653976654GA9GENIChomozygous126217533
12980537980538AT17GENIChomozygous126217535
12982422982423AG11GENIChomozygous126208008
12983205983206CT16GENIChomozygous126208011
12986049986050AG12GENIChomozygous126161128