chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96645467466454675GA22GENICheterozygous117369158
96645467666454677CT21GENICheterozygous117369160
96645467766454678GA21GENICheterozygous117369162
96645468666454687AG22GENICheterozygous117369164
96645480866454809CG29GENIChomozygous117369166
96645489466454895CG20GENIChomozygous117369168
96645490466454905TG18GENIChomozygous117369170
96645499666454997TA22GENIChomozygous117369172
96645503266455033TG15GENIChomozygous117369174
96645532266455323GA5GENIChomozygous117369176
96645557466455575GA7GENIChomozygous117369178
96645707866457079GA29GENIChomozygous117369180
96645771466457715CT39GENIChomozygous117369182
96645917966459180CT24GENICpossibly homozygous117369184
96646019666460197AG10GENIChomozygous117369186
96646076966460770CA15GENIChomozygous117369188
96646129666461297GA15GENIChomozygous117369190
96646244266462443GA47GENICheterozygous117369194
96646247466462475AG44GENIChomozygous117369196
96646259066462591GT62GENICheterozygous117369198
96646401366464014CT8GENIChomozygous117369200
96646466866464669GA15GENIChomozygous117369202
96646701266467013TC10GENIChomozygous117369204
96646741166467412GA11GENIChomozygous117369206
96646774166467742TC21GENIChomozygous117369208
96646942566469426GC26GENIChomozygous117369210
96646945666469457GA26GENIChomozygous117369212
96647000666470007AC13GENIChomozygous117369214
96647157666471577AG12GENIChomozygous117369216
96647259766472598GC19GENIChomozygous117369218
96647277866472779TG2GENIChomozygous117369220
96647510666475107TA27GENIChomozygous117369222
96647642666476427TA6GENIChomozygous117369224
96647694766476948GT30GENICheterozygous117369226
96647783466477835CT17GENIChomozygous117369228
96647922066479221TG11GENIChomozygous117369230
96648021766480218AG17GENIChomozygous117369231
96648029866480299GA19GENIChomozygous117369233
96648041066480411TG14GENIChomozygous117369235
96648102466481025GT25GENIChomozygous117369237
96648286566482866CT21GENIChomozygous117369241