chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6132586028132586029CT15GENICpossibly homozygous54723227
6132589742132589743TC24GENICpossibly homozygous54723232
6132589793132589796CTT---14GENICheterozygous54723234
6132590978132590979GA10GENICpossibly homozygous54723236
6132591604132591605GC10GENICpossibly homozygous54723246
6132592193132592194GGGT2GENICheterozygous54723250
6132592698132592699GA13GENICpossibly homozygous54723254
6132593010132593011AG3GENICheterozygous54723256
6132593900132593901CCAGAG2GENIChomozygous54723258
6132593993132593997GATT----5GENICheterozygous54987786
6132598330132598331TC7GENICheterozygous54723262
6132599819132599821AC--1GENIChomozygous54723266
6132599987132599988TTGGAGGCA2GENIChomozygous54723268
6132602795132602796TC17GENIChomozygous54723270
6132602819132602820AG21GENICpossibly homozygous54723272
6132603840132603841AG11GENIChomozygous54723274
6132604128132604129GA13GENICheterozygous54723277
6132607202132607203TC7GENICpossibly homozygous54723283
6132610550132610551GGC6GENICheterozygous54723290
6132610684132610685CT19GENIChomozygous54723292
6132610828132610829GA19GENICheterozygous54723294
6132611369132611370TC19GENIChomozygous54723295
6132611624132611625TG22GENIChomozygous54723297
6132611921132611922CT14GENIChomozygous54723299
6132600186132600187GGCTCTCT2GENICheterozygous55431990
6132605251132605252CCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTA8GENIChomozygous55431992