chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3121728229121728230CG68GENIChomozygous111690011
3121729643121729644GC49GENIChomozygous111690012
3121730387121730388TG71GENIChomozygous111690013
3121730622121730624TA55GENICheterozygous127924886
3121730795121730796TG61GENICpossibly homozygous111690015
3121732028121732029CA39GENIChomozygous111690016
3121732341121732342TC62GENIChomozygous111690017
3121732688121732822CCCCATGTCTGATTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTCCGGAGCTGGGGACCAAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC54GENIChomozygous127924887
3121733322121733324TA62GENIChomozygous127924888
3121737091121737096TCAGT67GENIChomozygous127924889