chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728380217283803TG23GENIChomozygous887568995
141728481617284817CT25GENIChomozygous887568996
141728489917284900CT26GENIChomozygous887568997
141728505217285053TA13GENIChomozygous887568998
141728505817285059CT13GENIChomozygous887568999
141728520317285204GC17GENIChomozygous887569000
141728533317285334TC6GENIChomozygous887569001
141728563217285633CT19GENIChomozygous887569002
141728587617285877CG12GENIChomozygous887569003
141728588117285882CT13GENIChomozygous887569004
141728604017286041GA12GENIChomozygous887569005
141728645617286457TC14GENIChomozygous887569006
141728669517286696CT17GENIChomozygous887569007
141728676817286769TA13GENIChomozygous887569008
141728677617286777TC12GENIChomozygous887569009
141728685817286859TC9GENIChomozygous887569010
141728751117287512TC8GENIChomozygous887569011
141729061517290616GT4GENICheterozygous887569012
141729113417291135GA21GENIChomozygous887569013
141729148217291483GC22GENIChomozygous887569014
141729201917292020CT25GENIChomozygous887569015
141729228617292287GC23GENIChomozygous887569016
141729295017292951CT19GENIChomozygous887569017
141729299117292992TC18GENICpossibly homozygous887569018
141729314017293141GA16GENIChomozygous887569019
141729327917293280AC17GENIChomozygous887569020
141729329117293292TC11GENIChomozygous887569021
141729348817293489AG14GENIChomozygous887569022
141729460317294604TC7GENICheterozygous887569023
141729472117294722AG22GENIChomozygous887569024
141729490717294908AG23GENIChomozygous887569025
141729502417295025TC15GENIChomozygous887569026
141729540917295410CT12GENIChomozygous887569027
141729542117295422GA12GENIChomozygous887569028
141729553717295538TC17GENIChomozygous887569029
141729591217295913TC13GENIChomozygous887569030
141729593717295938AG12GENIChomozygous887569031
141729638517296386AG20GENIChomozygous887569032
141729972117299722AG21GENIChomozygous887569033
141730108917301090TG16GENIChomozygous887569034
141730127317301274TC15GENIChomozygous887569035