chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6111477209111477210GC48GENIChomozygous807803141
6111477596111477597TG39GENIChomozygous807803142
6111477775111477776AG38GENIChomozygous807803143
6111477962111477963GC49GENICpossibly homozygous807803144
6111478157111478158GT32GENIChomozygous807803145
6111478175111478176GA31GENIChomozygous807803146
6111478376111478377TA27GENIChomozygous807803147
6111478447111478448CT33GENIChomozygous807803148
6111478449111478450GA35GENIChomozygous807803149
6111478551111478552CT28GENIChomozygous807803150
6111478766111478767AG45GENICpossibly homozygous807803151
6111478980111478981CT58GENICpossibly homozygous807803152
6111479360111479361CT48GENIChomozygous807803153
6111479664111479665AG31GENIChomozygous807803154
6111479806111479807GA37GENIChomozygous807803155
6111480069111480070CT65GENIChomozygous807803156
6111480093111480094AG54GENIChomozygous807803157
6111480357111480358CT61GENIChomozygous807803158
6111480406111480407GA61GENIChomozygous807803159
6111480449111480450GA65GENIChomozygous807803160
6111480611111480612TC51GENIChomozygous807803161
6111480630111480631TC46GENIChomozygous807803162
6111480894111480895CT49GENIChomozygous807803163
6111481514111481515GA71GENIChomozygous807803164
6111481601111481602AG78GENIChomozygous807803165
6111482451111482452GA37GENIChomozygous807803166
6111482981111482982TC65GENIChomozygous807803167
6111483352111483353AG47GENIChomozygous807803168
6111483811111483812CT39GENIChomozygous807803169
6111484855111484856GA49GENIChomozygous807803170
6111485417111485418TC51GENIChomozygous807803171
6111485516111485517CT35GENIChomozygous807803172
6111485625111485626AC41GENICpossibly homozygous807803173
6111485846111485847TC43GENIChomozygous807803174
6111486035111486036GA48GENIChomozygous807803175