chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2189089205189089206AG20INTERGENIChomozygous59299204
2189089518189089519A-42INTERGENIChomozygous59299205
2189090833189090834CT25INTERGENIChomozygous59299206
2189091069189091070TC5INTERGENIChomozygous59299207
2189091283189091284TG14INTERGENIChomozygous59299208
2189091638189091639GA4INTERGENIChomozygous59299209
2189092099189092100AC14INTERGENIChomozygous59299210
2189092137189092138GA10INTERGENIChomozygous59299211
2189092160189092161AT11INTERGENICpossibly homozygous59299212
2189092687189092688GA13INTERGENIChomozygous59299213
2189092720189092721TA18INTERGENIChomozygous59299214
2189093537189093538TG5INTERGENICheterozygous59299215
2189094019189094020AC15INTERGENIChomozygous59299216
2189094071189094072CCAT11INTERGENIChomozygous59299217
2189094374189094375TTTG7INTERGENICpossibly homozygous59299218
2189094750189094751CT15INTERGENIChomozygous59299219
2189095161189095162CA18INTERGENIChomozygous59299220
2189095736189095737AC24INTERGENICpossibly homozygous59299221
2189096352189096353TC23INTERGENICheterozygous59913167
2189096360189096361CT22INTERGENICheterozygous59913169
2189096409189096410CA35INTERGENICheterozygous60226634
2189096725189096726CT22INTERGENICpossibly homozygous59299225