chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103721608037216081TC12GENIChomozygous116562214
103721643337216434TA11GENIChomozygous116562216
103721664437216645CA5GENIChomozygous117170756
103721680637216807CT23GENIChomozygous116562218
103721688837216889CT26GENIChomozygous116562220
103721744937217450TC6GENIChomozygous116760059
103721771137217712TC20GENIChomozygous116562222
103721779937217800TC21GENIChomozygous116562224
103721817637218177TG3GENICheterozygous116562230
103721843237218433TA7GENIChomozygous116562234
103721897837218979TC20GENIChomozygous116562238
103721942737219428AC15GENIChomozygous116562240
103721956437219565AG23GENIChomozygous116562242
103721980637219807TC16GENIChomozygous116562244
103721995237219953TC17GENIChomozygous116562246
103722016037220161TG22GENIChomozygous116562248
103722026237220263CA6GENIChomozygous116562250
103722244637222447AG18GENIChomozygous116562252
103722310337223104AG10GENICheterozygous116562254
103722350437223505GA28GENIChomozygous116562256
103722364637223647CA14GENIChomozygous116562258
103722453637224537CG18GENIChomozygous116562260
103722494937224950GA24GENIChomozygous116562262
103722496637224967AG26GENIChomozygous116562264
103722516937225170AG21GENIChomozygous116562266
103722519637225197GC20GENIChomozygous116562268
103722534737225348TC13GENIChomozygous116562270
103722543437225435GA17GENIChomozygous116562272
103723869737238698AG23GENIChomozygous116562276
103724046437240465GA9GENIChomozygous116562278
103724124137241242AG21GENIChomozygous116562280