chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3116901408116901409CT77GENIChomozygous136797403
3116902182116902183AG52GENIChomozygous136797404
3116902266116902267AG62GENIChomozygous136797405
3116902912116902913TG57GENIChomozygous136797406
3116903142116903143CT62GENIChomozygous136797407
3116903841116903842GA68GENIChomozygous136797408
3116904241116904242TC53GENIChomozygous136797409
3116904246116904247TC52GENIChomozygous136797410
3116904873116904874GA42GENIChomozygous136797411
3116904944116904945AG47GENIChomozygous136797412
3116906568116906569CT65GENIChomozygous136797413
3116906773116906773TT45GENIChomozygous136585682
3116908498116908499AG50GENIChomozygous136797414
3116909083116909083TGAT63GENIChomozygous136585683
3116909433116909434TC64GENIChomozygous136797415
3116911349116911350GA41GENIChomozygous136797416
3116911813116911814CT58GENIChomozygous136797417
3116911822116911823CG57GENIChomozygous136797418
3116912063116912064A50GENICpossibly homozygous136585684
3116912065116912066GC51GENICpossibly homozygous136797419
3116912115116912116AG57GENIChomozygous136797420
3116912596116912597CG53GENIChomozygous136797421
3116912942116912943AG66GENIChomozygous136797422