chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4143425525143425526AT11GENICpossibly homozygous56962194
4143425716143425717GA14GENIChomozygous56962195
4143425764143425765TC9GENIChomozygous56962196
4143425767143425768AC8GENIChomozygous56962197
4143425781143425782TC7GENIChomozygous56962198
4143426721143426722A-7GENIChomozygous56962199
4143427870143427871GGTT4GENIChomozygous56962200
4143428102143428103GA4GENICheterozygous56962201
4143428326143428327T-7GENIChomozygous56962202
4143428627143428628GA13GENIChomozygous56962204
4143429113143429114CCATTT1GENIChomozygous56962206
4143429392143429393GA11GENICpossibly homozygous56962207
4143429465143429466TC8GENIChomozygous56962208
4143430684143430685AAAGTGTC1GENIChomozygous56962209
4143430722143430723TC3GENIChomozygous56962211
4143430885143430886GT12GENIChomozygous56962212
4143432424143432425TA12GENICheterozygous56962213
4143432605143432606GA15GENIChomozygous56962214