chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
387025488702549GA28GENIChomozygous111442056
387030468703047TC28GENIChomozygous111442057
387030718703072AG27GENIChomozygous111442058
387034978703498AG26GENIChomozygous111442060
387036148703615AG33GENIChomozygous111442061
387043438704344CT10GENIChomozygous111442062
387047208704721TG24GENIChomozygous111442063
387048818704882CT30GENIChomozygous111442064
387056038705604GA21GENIChomozygous111873138
387062028706203AG19GENIChomozygous111442065
387063558706356CT28GENIChomozygous111442066
387064428706443AG26GENIChomozygous111442067
387070538707054AG37GENIChomozygous111442068
387076258707626GA25GENIChomozygous111442069
387087028708703GC19GENIChomozygous111442070
387088428708843CT30GENIChomozygous112222991
387092338709234GA38GENIChomozygous111442071
387103698710370AT22GENIChomozygous111442072
387108358710836GA43GENIChomozygous111442073
387110618711062AG21GENIChomozygous111442074
387113028711303TC34GENIChomozygous111442075
387118538711854TC20GENIChomozygous111442076
387124458712446AG21GENIChomozygous111442077
387134968713497GA28GENIChomozygous111442078
387140838714084CT24GENIChomozygous111442080
387141518714152GT29GENIChomozygous111442081
387150708715071AG26GENIChomozygous111442082
387155918715592CT32GENIChomozygous111442083
387162998716300TC29GENIChomozygous111442084
387164398716440AG34GENIChomozygous111442085
387172048717205AT28GENIChomozygous111442086
387175798717580CT36GENIChomozygous111442087
387183188718319AG29GENIChomozygous111442088
387183548718355CT21GENIChomozygous111442089