chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108986384889863849CCAA9GENIChomozygous51735232
108986386889863869TA16GENICpossibly homozygous51735234
108986389589863897AA--17GENIChomozygous51537395
108986488889864889GGAAA15GENIChomozygous51735236
108986571789865718AAAAAAAG21GENIChomozygous51735238
108986637689866377CT47GENIChomozygous51735240
108986684789866848TTCA1GENIChomozygous51537397
108986803989868040CT49GENIChomozygous51735242
108986855389868554TC64GENIChomozygous51735244
108986907289869073AAT30GENIChomozygous51735246
108987025289870253TG24GENIChomozygous51735248
108987033789870338TG26GENICpossibly homozygous51735250
108987050589870506CT45GENIChomozygous51735252
108987056889870569CG30GENIChomozygous51735254
108987070889870709CT38GENIChomozygous51735256
108987077489870775GA48GENICpossibly homozygous51735258
108987122089871221GC38GENIChomozygous51735260
108987179689871797CA38GENIChomozygous51735262
108987190389871904TTC37GENIChomozygous51537398
108987383189873832TC18GENICpossibly homozygous51735264
108987383389873834AT17GENIChomozygous51735266
108987383689873857GAGAGTCCTAAGGCCCGAGTA---------------------8GENIChomozygous51735268
108987614589876146GA34GENICpossibly homozygous51735270
108987715689877157G-43GENIChomozygous51735272
108987755889877566GCGCGCGC--------11GENIChomozygous51735274
108987759489877595AACGCGCGCG19GENIChomozygous51735276
108987781689877817AATG28GENICheterozygous51735278
108987781689877817AATGTG28GENICpossibly homozygous51735280
108987826789878268AG52GENIChomozygous51735282
108987976789879768TTGC5GENIChomozygous51537399
108987983089879831AAT16GENICpossibly homozygous51735284
108988003489880035TC29GENIChomozygous51735286
108988013489880135TC42GENIChomozygous51735288
108988138789881389AA--37GENIChomozygous51735290