chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101359703113597032GC28GENIChomozygous116496318
101359821913598220AG27GENIChomozygous116496320
101359872013598721GA43GENIChomozygous116735883
101360057713600578AG13GENIChomozygous116496322
101360158513601586GA22GENICpossibly homozygous116735884
101360223313602234AG27GENIChomozygous116496325
101360403413604035AG19GENIChomozygous116496331
101360407313604074AC27GENIChomozygous116496333
101360447413604475TC34GENIChomozygous116735885
101360449613604497GA35GENIChomozygous116735886
101360485813604859TC28GENIChomozygous116496335
101360491713604918TC21GENIChomozygous116735887
101360511113605112TC20GENIChomozygous116496337
101360537513605376TC38GENIChomozygous116496339
101360561113605612CT31GENIChomozygous116496341
101360614713606148TC20GENIChomozygous116496343
101360623713606238AC22GENIChomozygous116496345
101360670813606709GC18GENIChomozygous116496347
101360728313607284GA34GENIChomozygous116735888
101360833813608339AT31GENIChomozygous116496349
101361026713610268AG26GENIChomozygous116735889
101361052013610521AG35GENIChomozygous116496353
101361062313610624AG39GENIChomozygous116496355
101361198113611982GA25GENIChomozygous116735892
101361223213612233GA21GENIChomozygous116735893
101361303013613031AG34GENIChomozygous116496365
101361319113613192GT34GENIChomozygous116496367
101361404113614042GA31GENIChomozygous116496369
101361433113614332GA37GENIChomozygous116496371
101361435213614353GA32GENIChomozygous116496373
101361492313614924GA43GENIChomozygous116496377
101361531413615315GA28GENIChomozygous116496379
101361573213615733CT26GENIChomozygous116735894
101361601313616014CG24GENIChomozygous116496381
101361639513616396AG33GENIChomozygous116496383
101361830813618309TC36GENIChomozygous116735895
101361839413618395AC33GENIChomozygous116735896
101361844913618450TC39GENIChomozygous116735897
101361850313618504AC42GENIChomozygous116735898
101361857313618574TC45GENIChomozygous116735899
101361862513618626AC43GENIChomozygous116735900