chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X6620916066209161TA4GENIChomozygous45380124
X6621110766211108GA19GENIChomozygous45380126
X6621224466212245CCTTAT4GENIChomozygous45380131
X6621384566213846AG10GENIChomozygous45380133
X6621466066214661G-8GENIChomozygous45145184
X6621466466214665G-7GENIChomozygous45145185
X6621466866214669GA7GENIChomozygous45145186
X6621475366214754CCTGTGTGTG3GENICheterozygous45478457
X6621475666214757TTGTGC3GENICheterozygous45858709
X6621629166216292AATAGT4GENIChomozygous45719529
X6621872266218723TA13GENIChomozygous45380137
X6621962866219629TC5GENIChomozygous45380139
X6622112466221125TC1GENIChomozygous45380141
X6622152766221528CT4GENIChomozygous45380143
X6622452866224529GA13GENIChomozygous45380145
X6622559666225597AG7GENIChomozygous45380147
X6622587666225879ATT---12GENICheterozygous45872605
X6622645166226452TC6GENIChomozygous45380149
X6622661566226616TTA1GENIChomozygous45380151
X6622734466227345AAGG4GENIChomozygous45380154
X6622747966227480AC9GENIChomozygous45380156
X6622763666227637GA7GENIChomozygous45380158
X6622799166227993AA--7GENIChomozygous45380160
X6622803566228036GGAA5GENIChomozygous45633337
X6622835766228358CCAA6GENIChomozygous45380162
X6622856066228561TA6GENIChomozygous45145187
X6623060166230607ATATAT------5GENIChomozygous45868476
X6623247366232474AAATAT7GENIChomozygous45380166
X6623254966232550AG3GENIChomozygous45380168
X6623281266232813T-5GENIChomozygous45380170
X6623323366233234TC4GENIChomozygous45380172
X6623435166234352TC2GENIChomozygous45380174