chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56907957369079574TA28INTERGENICheterozygous71391739
56908015669080157AG18INTERGENIChomozygous70670891
56908441969084420TA10INTERGENIChomozygous70670897
56908743869087439GA24INTERGENIChomozygous71391741
56908800369088004GT14INTERGENICpossibly homozygous71391743
56909042569090426CG6INTERGENIChomozygous70670909
56909129669091297CT18INTERGENIChomozygous70670912
56909145569091456GC29INTERGENIChomozygous70670915
56909191469091915TC15INTERGENIChomozygous70670921
56909216869092169AT19INTERGENIChomozygous70670924
56909019069090191AC9INTERGENIChomozygous72860173
56909244769092448CT19INTERGENICpossibly homozygous73893522
56909268369092684CT29INTERGENIChomozygous70670927
56909275669092757GA17INTERGENIChomozygous70670930
56909320769093208AC26INTERGENIChomozygous70670933
56909407769094078TC21INTERGENIChomozygous70670942
56909412169094122CT26INTERGENICpossibly homozygous72860179
56909412269094123AG26INTERGENIChomozygous70670948
56909419369094194AT19INTERGENICpossibly homozygous72860182
56909464669094647GA11INTERGENIChomozygous70670951
56909508969095090GA11INTERGENIChomozygous70670954
56909517769095178AG11INTERGENIChomozygous70670957
56909547169095472TC24INTERGENIChomozygous70670960
56909552769095528CT20INTERGENIChomozygous70670963
56909560569095606GT16INTERGENIChomozygous70670966
56909654969096550CG17INTERGENIChomozygous70670969
56909657969096580GA19INTERGENIChomozygous70670972
56909691269096913CT19INTERGENIChomozygous70670980
56909705869097059CT26INTERGENIChomozygous70670983
56909761469097615TA28INTERGENIChomozygous71391751