chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6132586028132586029CT15GENIChomozygous54723227
6132589742132589743TC11GENIChomozygous54723232
6132589793132589796CTT---8GENIChomozygous54723234
6132590978132590979GA10GENIChomozygous54723236
6132591553132591571TGTGTGTGTGTGTGTGTG------------------4GENIChomozygous55730976
6132591604132591605GC5GENIChomozygous54723246
6132592190132592191CCGG5GENICheterozygous54723248
6132592698132592699GA6GENIChomozygous54723254
6132593010132593011AG17GENIChomozygous54723256
6132593900132593901CCAGAG14GENIChomozygous54723258
6132597979132597980TTACAC7GENICheterozygous55730985
6132598040132598041GGGAGAGAGAGAGAGAGAGA2GENIChomozygous55540508
6132598330132598331TC12GENIChomozygous54723262
6132598526132598527A-8GENICpossibly homozygous54723264
6132599819132599821AC--10GENIChomozygous54723266
6132599987132599988TTGGAGGCA8GENIChomozygous54723268
6132600186132600187GGCTCTCT3GENIChomozygous55431990
6132602795132602796TC11GENIChomozygous54723270
6132602819132602820AG8GENIChomozygous54723272
6132603840132603841AG4GENIChomozygous54723274
6132604000132604001CCA16GENICpossibly homozygous54723275
6132604128132604129GA5GENIChomozygous54723277
6132604344132604345GA13GENIChomozygous54723279
6132605239132605240CCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTA6GENIChomozygous55730991
6132606575132606576GA12GENICheterozygous54987829
6132606580132606581TC12GENICheterozygous54987831
6132606946132606947GA4GENIChomozygous54723281
6132607202132607203TC13GENIChomozygous54723283
6132609031132609032GGCACA9GENICheterozygous54723285
6132609031132609032GGCA9GENICheterozygous54723287
6132610550132610551GGC8GENICpossibly homozygous54723290
6132610684132610685CT7GENIChomozygous54723292
6132610828132610829GA7GENIChomozygous54723294
6132611369132611370TC10GENIChomozygous54723295
6132611624132611625TG10GENIChomozygous54723297
6132611921132611922CT9GENIChomozygous54723299