chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56907950669079507TC19INTERGENIChomozygous70670888
56908015669080157AG16INTERGENIChomozygous70670891
56908424369084244AG22INTERGENIChomozygous70670894
56908441969084420TA15INTERGENIChomozygous70670897
56908948269089483CT22INTERGENIChomozygous70670903
56909017369090174TA16INTERGENIChomozygous70670906
56909042569090426CG13INTERGENIChomozygous70670909
56909129669091297CT20INTERGENIChomozygous70670912
56909191469091915TC23INTERGENIChomozygous70670921
56909216869092169AT11INTERGENIChomozygous70670924
56909268369092684CT15INTERGENIChomozygous70670927
56909275669092757GA19INTERGENIChomozygous70670930
56909320769093208AC24INTERGENIChomozygous70670933
56909407769094078TC16INTERGENIChomozygous70670942
56909409169094092CG14INTERGENIChomozygous70670945
56909412269094123AG14INTERGENIChomozygous70670948
56908900269089003GA13INTERGENICheterozygous72428081
56908926269089263TC16INTERGENIChomozygous72191416
56909005269090053GA21INTERGENIChomozygous72191418
56909028369090284CA11INTERGENIChomozygous72191420
56909225369092254GT23INTERGENICheterozygous72191422
56909464669094647GA7INTERGENIChomozygous70670951
56909508969095090GA11INTERGENIChomozygous70670954
56909517769095178AG7INTERGENIChomozygous70670957
56909519869095199CT8INTERGENIChomozygous72191424
56909542969095430CT16INTERGENIChomozygous72191426
56909547169095472TC18INTERGENIChomozygous70670960
56909552769095528CT16INTERGENIChomozygous70670963
56909556069095561TC11INTERGENIChomozygous72191428
56909615069096151CT18INTERGENIChomozygous72191430
56909654969096550CG9INTERGENIChomozygous70670969
56909688869096889CT15INTERGENIChomozygous72191432
56909691269096913CT12INTERGENIChomozygous70670980
56909735869097359GA9INTERGENIChomozygous72191434
56909610469096104A20INTERGENICheterozygous72965060