chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85928050959280510AC29GENIChomozygous52982979
85928069359280699GCTGCT------6GENIChomozygous52663254
85928079659280797AG28GENIChomozygous52663256
85928084459280845AC37GENIChomozygous52982980
85928250159282502GT21GENICpossibly homozygous52982981
85928254659282549GAA---16GENICheterozygous52982982
85928254759282548A-9GENICheterozygous52663258
85928257059282571A-1GENIChomozygous52663260
85928345959283460A-14GENICheterozygous52663262
85928384659283847TC44GENICpossibly homozygous52663264
85928704059287043AAA---11GENIChomozygous52982983
85928732359287324AG57GENIChomozygous52982984
85928744059287441TA40GENIChomozygous52982985
85928788359287913ATGTTGTTTTCCTTACCAAGTACTCAGTAC------------------------------3GENIChomozygous52982986
85928800159288002TC19GENIChomozygous52663270
85928853859288540GA--40GENIChomozygous52663272
85928888959288892GGG---8GENICheterozygous52663274
85928891059288915GGGTC-----4GENICheterozygous52663276
85928930359289304GT39GENIChomozygous52663280
85928968059289681CT38GENIChomozygous52982987
85929067259290673CA49GENIChomozygous52663284
85929110259291103TC45GENIChomozygous52663288
85929163259291633T-1GENIChomozygous53182125
85929427159294272CT47GENIChomozygous52663290
85929450959294510AAG34GENIChomozygous52663291
85929460159294602TA42GENIChomozygous52982988
85929462159294622GT45GENIChomozygous52663293
85929520759295226TGTGTGTGTGTGTGTGTGT-------------------22GENICheterozygous52663295
85929522759295228T-14GENICheterozygous52663297
85929639759296398CT38GENICpossibly homozygous52982989
85929747559297476AG43GENIChomozygous52663301