chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81128000511280006AC41GENIChomozygous142034254
81128087811280879TC43GENIChomozygous142034255
81128487411284875CT45GENIChomozygous142034256
81128487511284876AG47GENIChomozygous142034257
81128567611285677CT55GENIChomozygous142034258
81128640311286404T50GENIChomozygous142016920
81128740111287402GC67GENIChomozygous142034259
81128771711287718AG56GENIChomozygous142034260
81128776411287765CT66GENIChomozygous142034261
81128913311289134GA63GENIChomozygous142034262
81128944511289446CT54GENIChomozygous142034263
81128987211289873AG47GENIChomozygous142034264
81129120111291202AG60GENIChomozygous142034265
81129157711291578CT72GENICpossibly homozygous142034266
81129226611292267GA60GENIChomozygous142034267
81129324311293245CA29GENICheterozygous146461821
81129324611293273ATGTATGCTGAGTATTGATACTCTGTC32GENICheterozygous146461822
81129353211293533CT63GENIChomozygous142034268
81129493211294933A40GENIChomozygous142016921
81129520811295208C39GENIChomozygous142016922
81129559811295598A60GENICpossibly homozygous142016923
81129859411298604GGTGAGGTGA13GENIChomozygous142016924
81129928011299320GGTGAGGTGAGGTGAGGTGAGGTGAGGTGAGGTGCGGTGA18GENIChomozygous142016927
81130055011300551C36GENIChomozygous142016928
81130117111301175ATGT38GENIChomozygous142016929
81130145411301455T46GENIChomozygous142016930
81130326511303266T46GENIChomozygous142016931
81129871611298717G5GENICheterozygous404005696
81129543711295438GA53GENIChomozygous142034269
81130371111303712CT54GENIChomozygous142034270
81130412911304130GT47GENIChomozygous142034271
81130443211304433AG19GENIChomozygous142034272
81130445011304451GA30GENIChomozygous142034273
81129871611298717GA5GENIChomozygous154506504