chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141634208916342090GA75GENIChomozygous113808748
141634213416342135CT62GENIChomozygous113808750
141634233316342334CA49GENIChomozygous114042041
141634302116343022GA53GENIChomozygous113808752
141634564416345645GT54GENIChomozygous113808754
141634658416346585GA44GENIChomozygous113808756
141634408716344088A48GENIChomozygous133271915
141634664316346644AG51GENIChomozygous113358085
141634556716345568AG60GENIChomozygous113358081
141634723216347233TC65GENIChomozygous113358088
141634773616347737TC65GENIChomozygous113808758
141634945416349455CT57GENIChomozygous113808760
141635026716350268CT52GENIChomozygous113808762
141635166716351668TC51GENICpossibly homozygous113808764
141635211216352113TC42GENIChomozygous113358096
141635267816352678TTCCTAAAGAT56GENIChomozygous129128585
141635475016354751AG47GENIChomozygous113358098
141635629116356291GGA57GENIChomozygous129128587
141635630516356306CT66GENIChomozygous113808766
141635715816357159GA51GENIChomozygous113808768
141635780216357803CT56GENIChomozygous113808770
141635828716358288T62GENIChomozygous133271916
141635999216359992CACATGTATGTGA37GENIChomozygous133271917
141636039316360394TC54GENIChomozygous113358108
141636109216361093TC51GENIChomozygous113358110
141636132916361330CT49GENIChomozygous113808772
141636164216361642CTGTCAGAAT48GENIChomozygous129128588
141636164416361644GA46GENIChomozygous129128589
141636178016361781TA54GENIChomozygous113808774
141636244716362448GT53GENIChomozygous113808776
141636374816363749GA56GENIChomozygous113808778
141636397416363975GA46GENIChomozygous113808780