chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13106481083106481084CT20GENIChomozygous143597141
13106481122106481123GA20GENIChomozygous143597142
13106481409106481410GC22GENIChomozygous143597143
13106481773106481774CT27GENIChomozygous143597144
13106481989106481990CT22GENIChomozygous143597145
13106482444106482445AG23GENICpossibly homozygous139371534
13106482872106482873TC26GENIChomozygous143597146
13106483758106483759AG17GENIChomozygous139371536
13106483844106483845TC20GENIChomozygous139371537
13106484181106484182AG23GENIChomozygous139371539
13106484422106484423TC28GENIChomozygous139371540
13106485667106485668CT20GENIChomozygous143597147
13106486553106486554GA25GENIChomozygous143597148
13106487520106487521GA12GENIChomozygous143597149
13106487694106487695TC29GENIChomozygous143597150
13106487820106487821CG20GENIChomozygous139371541
13106482798106482799A23GENIChomozygous141096281
13106488349106488350TC19GENIChomozygous139371542
13106489888106489889TC17GENIChomozygous139371545
13106491469106491470CT17GENIChomozygous143597151
13106491476106491477TA17GENIChomozygous143597152
13106492553106492554GA18GENIChomozygous143597153
13106484784106484785TC10GENIChomozygous154796685
13106484784106484785T10GENICheterozygous403849888
13106493585106493586GA27GENIChomozygous143597154
13106494308106494309TC28GENIChomozygous143597155
13106495130106495131T19GENICheterozygous404443953
13106495130106495131TC19GENICheterozygous404443954
13106495494106495495CT20GENIChomozygous143597156
13106492935106492935C23GENIChomozygous143553699
13106496296106496297TG12GENIChomozygous143597157
13106497375106497376CT12GENIChomozygous143597158
13106498914106498915CT18GENIChomozygous143597159
13106499216106499226CCTCACAGTA22GENIChomozygous143553700
13106494425106494426T24GENICpossibly homozygous139192225