chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
38181486881814869G17GENIChomozygous127901416
38181657481816575TC14GENIChomozygous111637178
38181991481819914C19GENIChomozygous127901417
38182070081820700C21GENIChomozygous127901418
38182123781821238GC20GENIChomozygous111637179
38182273381822734CT18GENIChomozygous111637181
38182591581825916AG11GENIChomozygous111637182
38182698481826985CT19GENIChomozygous111637184
38182825281828253AG19GENIChomozygous111637185
38182898981828990GA14GENIChomozygous111637187
38183013281830133GA23GENIChomozygous111637189
38183121681831217GA15GENIChomozygous111637190
38183122081831221AC14GENIChomozygous111637192
38183139781831398TC12GENIChomozygous111637193
38183150181831502TC16GENIChomozygous111637195
38183254381832545TT14GENIChomozygous127901419
38183408581834086CT17GENIChomozygous111637197
38183524581835246AC21GENIChomozygous111637198
38182253281822533TC9GENIChomozygous119701585
38183579481835794A7GENIChomozygous127901420
38183633081836331CT17GENIChomozygous111637203
38183669681836697AG13GENIChomozygous111637204
38183881481838815CT16GENIChomozygous111637206
38183934281839343TC16GENIChomozygous111637208
38184008081840080A14GENIChomozygous127901421
38184176081841761CT13GENIChomozygous111637209
38184278181842782AG25GENIChomozygous111637211
38184298881842988AAGG13GENIChomozygous127901422
38184303481843035TA13GENIChomozygous111637212
38184561381845614AT16GENIChomozygous111637214
38184604981846051AC13GENIChomozygous127901423
38184691881846919TG11GENIChomozygous111637216
38184698081846981TC12GENIChomozygous111637217
38184750081847501GA12GENIChomozygous111637219
38185010781850108GA19GENIChomozygous111637220
38185101681851017CT10GENIChomozygous111637222
38185102381851024T9GENIChomozygous127901427
38185180381851804A10GENIChomozygous127901428
38185199681851997TA24GENIChomozygous111637224