chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135144913135144914A21GENIChomozygous137343627
5135146545135146546GC19GENIChomozygous137629395
5135147240135147241AG18GENIChomozygous137629396
5135148256135148256CAAACAAG15GENIChomozygous137343628
5135148829135148830TC18GENIChomozygous137629397
5135148961135148962TG16GENIChomozygous137629398
5135151974135151975TC18GENIChomozygous137629402
5135150495135150496GA15GENIChomozygous137629399
5135151938135151939TC19GENIChomozygous137629400
5135151963135151964GA19GENIChomozygous137629401
5135152190135152191TC21GENIChomozygous137629403
5135152384135152385GA15GENIChomozygous137629404
5135153586135153587AG16GENIChomozygous137629405
5135155307135155308TC13GENIChomozygous137629406
5135155900135155901GA14GENIChomozygous137629407
5135156005135156006CT17GENIChomozygous137629408
5135156014135156015CT16GENIChomozygous137629409
5135156018135156024CACATC16GENIChomozygous137343629
5135156025135156026TA16GENIChomozygous137629410
5135156028135156036ACATTATA15GENIChomozygous137343630
5135156475135156476GC18GENIChomozygous137629411
5135157243135157246TAA13GENIChomozygous137343631
5135157293135157294A15GENIChomozygous137343632
5135157762135157763TC12GENIChomozygous137629412
5135158844135158845GA17GENIChomozygous137629413
5135159418135159419GT22GENIChomozygous137629414
5135159712135159713AT20GENIChomozygous137629415
5135166023135166024AG11GENIChomozygous137629416
5135167261135167262GC20GENIChomozygous137629417
5135156023135156024CT16GENICheterozygous154324677
5135156023135156024C16GENIChomozygous403159216
5135157841135157842C16GENIChomozygous137343633