chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1257868592257868593TC56GENIChomozygous135879133
1257872843257872844AG50GENIChomozygous135879134
1257873308257873309GA50GENICpossibly homozygous135879135
1257876808257876809TC24GENIChomozygous135879136
1257877292257877293CT51GENIChomozygous135879137
1257878130257878132TG36GENICheterozygous146595618
1257874619257874619GGTGCATGTGTATATAGGTGTTCATGGGGTGTATGTGTAGGGGTACGTGTGTGTAGGAGTGCATGTGTGTGTAGA16GENIChomozygous135475848
1257876646257876767ACTTTCTATTCACTCAAAAGGGCTTGGGTGGCCTCTATGCAAATATTAAAGCTATACGTCTGGACTTTGATCGCTCCATCAGCAATGGAGAGTAGTTAAGGCCAGGTCAAGAGGTTTGTAT15GENIChomozygous135475849
1257878108257878110TC43GENIChomozygous135475850
1257878133257878134GC36GENICheterozygous146633755
1257878280257878282GT48GENIChomozygous135475851
1257878284257878285TC49GENIChomozygous135879138
1257878286257878287C49GENIChomozygous135475852
1257878299257878300CT49GENIChomozygous135879139
1257878999257879000G47GENIChomozygous135475853
1257879125257879126CG57GENIChomozygous135879140
1257879899257879900AG60GENIChomozygous135879141
1257880566257880567AG65GENIChomozygous135879142
1257881599257881600CT52GENIChomozygous135879143
1257883048257883049CA49GENIChomozygous135879144