chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155915597155915598A39GENIChomozygous131392529
5155915975155915976GA49GENIChomozygous119185280
5155917509155917509A21GENIChomozygous128261739
5155916920155916921AG39GENIChomozygous114066165
5155917448155917449G16GENIChomozygous128261736
5155917455155917455T17GENIChomozygous128261737
5155917492155917492A22GENIChomozygous128261738
5155917609155917609T11GENIChomozygous128261740
5155917632155917633C6GENIChomozygous128261741
5155917647155917648C7GENIChomozygous128261742
5155917658155917659A7GENIChomozygous128261743
5155917682155917682T7GENIChomozygous128261744
5155917692155917693TA7GENIChomozygous114066167
5155917700155917700T7GENIChomozygous128261745
5155917704155917704A5GENIChomozygous128261746
5155917724155917724G8GENIChomozygous128261747
5155918900155918901AG43GENIChomozygous114066169
5155919313155919314CT32GENIChomozygous114066171
5155919390155919391TC30GENIChomozygous114066173
5155919624155919624GGGA12GENIChomozygous128261748
5155919827155919828AT32GENICpossibly homozygous114066177
5155920055155920056TG38GENICpossibly homozygous114066179
5155920089155920090GA37GENIChomozygous114066181
5155920122155920123CG44GENIChomozygous114066183
5155920211155920212GA34GENIChomozygous114066185
5155920281155920282GA32GENIChomozygous114066187
5155920568155920573AAAAG36GENIChomozygous128261749
5155920725155920725GATGGTGATGAT40GENIChomozygous131392530
5155920735155920736CA46GENIChomozygous114066189
5155920738155920739CA47GENIChomozygous114066191
5155921056155921057CT45GENIChomozygous114066198
5155921483155921483GTTTTGTTTTT41GENIChomozygous128261751
5155921737155921738GA41GENIChomozygous114066200
5155921958155921959CT46GENIChomozygous114066202
5155919629155919630AG10GENIChomozygous119204559