chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56907955969079560TA22INTERGENICheterozygous71391737
56907957369079574TA24INTERGENICheterozygous71391739
56907963069079631CT30INTERGENICheterozygous71916497
56908015669080157AG41INTERGENIChomozygous70670891
56908441969084420TA34INTERGENIChomozygous70670897
56908743869087439GA25INTERGENIChomozygous71391741
56908800369088004GT24INTERGENICpossibly homozygous71391743
56908982969089830GA30INTERGENIChomozygous71391745
56909038169090382GA22INTERGENICheterozygous71391747
56909129669091297CT34INTERGENIChomozygous70670912
56909145569091456GC26INTERGENIChomozygous70670915
56909182769091828GA32INTERGENIChomozygous70670918
56909191469091915TC32INTERGENIChomozygous70670921
56909216869092169AT23INTERGENIChomozygous70670924
56909268369092684CT27INTERGENIChomozygous70670927
56909275669092757GA23INTERGENIChomozygous70670930
56909320769093208AC30INTERGENIChomozygous70670933
56909356969093570CT40INTERGENIChomozygous70670936
56909407769094078TC41INTERGENIChomozygous70670942
56909409169094092CG35INTERGENICpossibly homozygous70670945
56909412269094123AG32INTERGENIChomozygous70670948
56909464669094647GA27INTERGENIChomozygous70670951
56909508969095090GA37INTERGENIChomozygous70670954
56909517769095178AG29INTERGENIChomozygous70670957
56909547169095472TC27INTERGENIChomozygous70670960
56909552769095528CT23INTERGENIChomozygous70670963
56909560569095606GT40INTERGENIChomozygous70670966
56909580169095802TA37INTERGENIChomozygous71391749
56909654969096550CG20INTERGENIChomozygous70670969
56909657969096580GA20INTERGENIChomozygous70670972
56909668669096687CT28INTERGENICheterozygous70670974
56909679569096796CT40INTERGENICheterozygous70670977
56909691269096913CT22INTERGENIChomozygous70670980
56909705869097059CT32INTERGENIChomozygous70670983
56909761469097615TA20INTERGENIChomozygous71391751