chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104532413945324140TTCAGATACTGTGTAGATCGCTTCTCGGCCTTTTGGCTAAGATCAAGTG1GENIChomozygous52372925
104532417045324171TTACTC5GENIChomozygous51442213
104532507245325075GGT---1GENIChomozygous51442216
104532520745325208GA23GENICpossibly homozygous51442217
104532791145327912AAAC3GENIChomozygous51442218
104532842845328429CT19GENICpossibly homozygous51442219
104532913945329140CT19GENIChomozygous51442220
104533061845330619CCGT1GENIChomozygous51442225
104533412245334123AT2GENIChomozygous51442228