chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108905096689050967GT26GENICpossibly homozygous51731312
108905112489051125TG26GENIChomozygous51731314
108905194189051942CT20GENIChomozygous51731322
108905222089052221CT22GENICpossibly homozygous51731324
108905270489052813AGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAGAAAGAAAGAATA-------------------------------------------------------------------------------------------------------------1GENIChomozygous52323007
108905297989052980AAT1GENIChomozygous51731344
108905313289053133AG13GENICpossibly homozygous51731346
108905313789053138CA12GENICpossibly homozygous51731348
108905347089053471AT10GENICpossibly homozygous52574128
108905352889053642CTGAATATTACAATTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC------------------------------------------------------------------------------------------------------------------8GENIChomozygous52323009
108905380589053806GA24GENIChomozygous51731356
108905431089054311GA28GENIChomozygous52574131
108905439089054391GC16GENICpossibly homozygous52574134
108905509889055099CT16GENIChomozygous51731362
108905518689055187CT24GENIChomozygous51731364
108905578289055783TC21GENICpossibly homozygous51731366
108905639789056398AG26GENIChomozygous52574137
108905717489057175GA15GENIChomozygous51731370