chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
387025488702549GA24GENIChomozygous111442056
387030468703047TC12GENIChomozygous111442057
387030718703072AG22GENIChomozygous111442058
387034978703498AG16GENIChomozygous111442060
387036148703615AG28GENIChomozygous111442061
387043438704344CT16GENIChomozygous111442062
387047208704721TG26GENIChomozygous111442063
387048818704882CT15GENIChomozygous111442064
387056038705604GA7GENICheterozygous111873138
387062028706203AG16GENIChomozygous111442065
387063558706356CT13GENIChomozygous111442066
387064428706443AG10GENIChomozygous111442067
387076258707626GA22GENIChomozygous111442069
387087028708703GC17GENIChomozygous111442070
387090888709089TA19GENICpossibly homozygous119647584
387092338709234GA22GENIChomozygous111442071
387103698710370AT13GENIChomozygous111442072
387108358710836GA27GENIChomozygous111442073
387110618711062AG9GENIChomozygous111442074
387113028711303TC17GENIChomozygous111442075
387118538711854TC19GENIChomozygous111442076
387124458712446AG13GENIChomozygous111442077
387134968713497GA10GENIChomozygous111442078
387135148713515GA9GENIChomozygous111442079
387140838714084CT26GENIChomozygous111442080
387141518714152GT18GENIChomozygous111442081
387150708715071AG24GENIChomozygous111442082
387155918715592CT23GENIChomozygous111442083
387162998716300TC11GENIChomozygous111442084
387164398716440AG8GENIChomozygous111442085
387172048717205AT12GENIChomozygous111442086
387175798717580CT14GENIChomozygous111442087
387183188718319AG6GENIChomozygous111442088
387183548718355CT12GENIChomozygous111442089