chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108986384889863849CCAA2GENIChomozygous51735232
108986389589863897AA--6GENIChomozygous51537395
108986488889864889GGAAA12GENIChomozygous51735236
108986571789865718AAAAAAAG17GENICpossibly homozygous51735238
108986637689866377CT26GENIChomozygous51735240
108986684789866848TTCA6GENIChomozygous51537397
108986803989868040CT22GENIChomozygous51735242
108986855389868554TC22GENIChomozygous51735244
108986907289869073AAT24GENIChomozygous51735246
108987025289870253TG21GENIChomozygous51735248
108987033789870338TG25GENIChomozygous51735250
108987050589870506CT27GENIChomozygous51735252
108987056889870569CG27GENIChomozygous51735254
108987070889870709CT28GENIChomozygous51735256
108987077489870775GA30GENIChomozygous51735258
108987122089871221GC27GENIChomozygous51735260
108987179689871797CA30GENIChomozygous51735262
108987190389871904TTC33GENIChomozygous51537398
108987240489872405AT3GENICheterozygous51997543
108987240889872409CT3GENICheterozygous51997545
108987240989872410CT3GENICheterozygous51997548
108987383189873832TC16GENIChomozygous51735264
108987383389873834AT14GENICpossibly homozygous51735266
108987383689873857GAGAGTCCTAAGGCCCGAGTA---------------------4GENIChomozygous51735268
108987614589876146GA16GENIChomozygous51735270
108987715689877157G-18GENIChomozygous51735272
108987755889877566GCGCGCGC--------8GENIChomozygous51735274
108987759489877595AACGCGCGCG18GENICpossibly homozygous51735276
108987759889877599AG18GENICpossibly homozygous51928115
108987781689877817AATGTG15GENIChomozygous51735280
108987826789878268AG8GENIChomozygous51735282
108987976789879768TTGC2GENIChomozygous51537399
108987983089879831AAT15GENIChomozygous51735284
108988003489880035TC28GENIChomozygous51735286
108988013489880135TC22GENIChomozygous51735288
108988138789881389AA--29GENIChomozygous51735290