chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56907957369079574TA23INTERGENICpossibly homozygous71391739
56908015669080157AG20INTERGENIChomozygous70670891
56908441969084420TA31INTERGENIChomozygous70670897
56908743869087439GA24INTERGENIChomozygous71391741
56908800369088004GT32INTERGENIChomozygous71391743
56908903369089034CT10INTERGENICheterozygous70670900
56908982969089830GA18INTERGENIChomozygous71391745
56909129669091297CT24INTERGENIChomozygous70670912
56909145569091456GC27INTERGENIChomozygous70670915
56909182769091828GA23INTERGENIChomozygous70670918
56909191469091915TC12INTERGENIChomozygous70670921
56909216869092169AT14INTERGENIChomozygous70670924
56909268369092684CT19INTERGENIChomozygous70670927
56909275669092757GA17INTERGENIChomozygous70670930
56909320769093208AC31INTERGENIChomozygous70670933
56909356969093570CT29INTERGENIChomozygous70670936
56909407769094078TC19INTERGENIChomozygous70670942
56909409169094092CG20INTERGENIChomozygous70670945
56909412269094123AG15INTERGENIChomozygous70670948
56909464669094647GA15INTERGENIChomozygous70670951
56909508969095090GA21INTERGENIChomozygous70670954
56909517769095178AG22INTERGENIChomozygous70670957
56909547169095472TC22INTERGENIChomozygous70670960
56909552769095528CT26INTERGENIChomozygous70670963
56909560569095606GT21INTERGENIChomozygous70670966
56909580169095802TA26INTERGENIChomozygous71391749
56909654969096550CG8INTERGENIChomozygous70670969
56909657969096580GA7INTERGENIChomozygous70670972
56909691269096913CT19INTERGENIChomozygous70670980
56909705869097059CT27INTERGENIChomozygous70670983
56909761469097615TA17INTERGENIChomozygous71391751