chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161996858719968588AC2GENIChomozygous47325448
161996867319968674TC3GENIChomozygous47325452
161996997419969975TTG7GENIChomozygous47627222
161997040519970406TC15GENICpossibly homozygous47627224
161997065019970651AG7GENICpossibly homozygous47325454
161997078219970783CT6GENIChomozygous47325456
161997268119972682TTTC7GENICheterozygous47627226
161997272919972730AC14GENIChomozygous47627228
161997292119972922CG2GENIChomozygous47627230
161997303619973037AG5GENIChomozygous47627232
161997346019973461TTGG1GENIChomozygous47627236
161997349619973497AT15GENIChomozygous47627238
161997363119973632T-5GENIChomozygous47325460
161997385719973858AG7GENICpossibly homozygous47627240
161997426619974267CT16GENIChomozygous47627242
161997491319974914TC13GENICpossibly homozygous47627244
161997536819975369CT4GENIChomozygous47627248
161997543119975432CT19GENICpossibly homozygous47627250
161997600919976010AG15GENIChomozygous47627252
161997606919976070AG18GENIChomozygous47627254
161997905919979060C-14GENIChomozygous47325482
161997937519979376CA9GENICpossibly homozygous47627256
161998036719980368AT20GENICpossibly homozygous47325492
161998037819980379AG17GENIChomozygous47325494
161998064819980649AG2GENIChomozygous47325496