chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56907957369079574TA24INTERGENICheterozygous71391739
56908015669080157AG17INTERGENIChomozygous70670891
56908441969084420TA35INTERGENIChomozygous70670897
56908743869087439GA31INTERGENIChomozygous71391741
56908800369088004GT22INTERGENIChomozygous71391743
56908903369089034CT17INTERGENICheterozygous70670900
56908982969089830GA20INTERGENIChomozygous71391745
56909129669091297CT12INTERGENIChomozygous70670912
56909145569091456GC25INTERGENIChomozygous70670915
56909182769091828GA19INTERGENIChomozygous70670918
56909191469091915TC23INTERGENIChomozygous70670921
56909216869092169AT20INTERGENIChomozygous70670924
56909268369092684CT23INTERGENIChomozygous70670927
56909275669092757GA22INTERGENIChomozygous70670930
56909320769093208AC27INTERGENIChomozygous70670933
56909356969093570CT30INTERGENIChomozygous70670936
56909407769094078TC19INTERGENIChomozygous70670942
56909409169094092CG17INTERGENIChomozygous70670945
56909412269094123AG20INTERGENIChomozygous70670948
56909464669094647GA17INTERGENIChomozygous70670951
56909508969095090GA22INTERGENIChomozygous70670954
56909517769095178AG17INTERGENIChomozygous70670957
56909547169095472TC41INTERGENIChomozygous70670960
56909552769095528CT29INTERGENIChomozygous70670963
56909560569095606GT28INTERGENIChomozygous70670966
56909580169095802TA24INTERGENIChomozygous71391749
56909654969096550CG14INTERGENIChomozygous70670969
56909657969096580GA11INTERGENIChomozygous70670972
56909691269096913CT16INTERGENIChomozygous70670980
56909705869097059CT19INTERGENIChomozygous70670983
56909761469097615TA17INTERGENIChomozygous71391751