chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56907957369079574TA13INTERGENICheterozygous71391739
56908015669080157AG25INTERGENIChomozygous70670891
56908441969084420TA21INTERGENIChomozygous70670897
56908743869087439GA18INTERGENIChomozygous71391741
56908800369088004GT19INTERGENIChomozygous71391743
56908903369089034CT5INTERGENICheterozygous70670900
56908982969089830GA17INTERGENICpossibly homozygous71391745
56909129669091297CT21INTERGENIChomozygous70670912
56909145569091456GC28INTERGENIChomozygous70670915
56909182769091828GA20INTERGENIChomozygous70670918
56909191469091915TC16INTERGENIChomozygous70670921
56909216869092169AT27INTERGENIChomozygous70670924
56909268369092684CT25INTERGENIChomozygous70670927
56909275669092757GA14INTERGENIChomozygous70670930
56909320769093208AC18INTERGENIChomozygous70670933
56909356969093570CT24INTERGENIChomozygous70670936
56909407769094078TC21INTERGENIChomozygous70670942
56909409169094092CG17INTERGENIChomozygous70670945
56909412269094123AG21INTERGENIChomozygous70670948
56909464669094647GA24INTERGENIChomozygous70670951
56909508969095090GA26INTERGENIChomozygous70670954
56909517769095178AG24INTERGENIChomozygous70670957
56909547169095472TC16INTERGENIChomozygous70670960
56909552769095528CT21INTERGENIChomozygous70670963
56909560569095606GT22INTERGENIChomozygous70670966
56909580169095802TA14INTERGENIChomozygous71391749
56909654969096550CG17INTERGENIChomozygous70670969
56909657969096580GA18INTERGENIChomozygous70670972
56909691269096913CT25INTERGENIChomozygous70670980
56909705869097059CT15INTERGENIChomozygous70670983
56909761469097615TA12INTERGENIChomozygous71391751