chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38181486881814869G43GENIChomozygous127901416
38181657481816575TC50GENIChomozygous111637178
38181991481819914C62GENIChomozygous127901417
38182070081820700C41GENIChomozygous127901418
38182123781821238GC22GENIChomozygous111637179
38182253281822533TC27GENIChomozygous119701585
38182273381822734CT62GENIChomozygous111637181
38182591581825916AG43GENIChomozygous111637182
38182698481826985CT53GENIChomozygous111637184
38182825281828253AG67GENIChomozygous111637185
38182898981828990GA65GENIChomozygous111637187
38183013281830133GA66GENIChomozygous111637189
38183121681831217GA57GENIChomozygous111637190
38183122081831221AC60GENIChomozygous111637192
38183139781831398TC40GENIChomozygous111637193
38183150181831502TC43GENIChomozygous111637195
38183254381832545TT53GENIChomozygous127901419
38183408581834086CT52GENIChomozygous111637197
38183524581835246AC53GENIChomozygous111637198
38183579481835794A48GENIChomozygous127901420
38183633081836331CT64GENIChomozygous111637203
38183669681836697AG68GENIChomozygous111637204
38183881481838815CT63GENIChomozygous111637206
38183934281839343TC60GENIChomozygous111637208
38184008081840080A48GENICpossibly homozygous127901421
38184176081841761CT57GENIChomozygous111637209
38184278181842782AG69GENIChomozygous111637211
38184298881842988AAGG51GENIChomozygous127901422
38184303481843035TA62GENIChomozygous111637212
38184561381845614AT57GENIChomozygous111637214
38184604981846051AC41GENIChomozygous127901423
38184636181846361ACC14GENICheterozygous127901424
38184691881846919TG69GENIChomozygous111637216
38184698081846981TC70GENIChomozygous111637217
38184750081847501GA70GENIChomozygous111637219
38185010781850108GA60GENIChomozygous111637220
38185101681851017CT65GENIChomozygous111637222
38185102381851024T67GENIChomozygous127901427
38185180381851804A47GENIChomozygous127901428
38185199681851997TA63GENIChomozygous111637224