chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124247956142479562AT17GENIChomozygous50209153
124247956642479567TG17GENIChomozygous50209154
124247957242479573TC18GENIChomozygous50209155
124248066042480661CCCA5GENICheterozygous50209156
124248066042480661CCCACA5GENICheterozygous50544348
124248311442483157AGATGGGTGCTCTTAACCGCTGAGCCATCTCTCCAGCCCCCCC-------------------------------------------9GENICheterozygous50544349
124248336842483369T-16GENICheterozygous50563858
124248395142483952G-5GENIChomozygous50209157
124248470742484708CT24GENIChomozygous50209161
124248501342485014T-10GENIChomozygous50544350
124248501542485026TGTGTGTGTGT-----------10GENICpossibly homozygous50544351
124248766542487666AC17GENIChomozygous50209167
124248770642487707CT20GENIChomozygous50209168
124248772942487730TC21GENIChomozygous50209169
124248811342488114AATTTTT4GENICheterozygous50544352
124248841242488421TTTTTTTAA---------5GENICheterozygous50209173
124248897242488973GA27GENIChomozygous50209174
124249034742490348TA32GENIChomozygous50209175
124249053842490539AG14GENIChomozygous50209176
124249060142490602GA3GENIChomozygous50544353
124249060242490603CCACACACACA4GENICheterozygous50209179
124249060242490603CCACACACA4GENICheterozygous50544354
124249065742490658CT20GENIChomozygous50209180
124249139342491394CT12GENIChomozygous50209181
124249410142494102CA20INTERGENIChomozygous50209183
124249415742494158AG26INTERGENIChomozygous50209184