chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103772620837726209GT25GENIChomozygous116562899
103772693837726939AC9GENIChomozygous116760361
103772693937726940GA8GENIChomozygous116760363
103772807237728073TC19GENIChomozygous116562903
103772940937729410TC16GENIChomozygous116562907
103772953137729532CT16GENIChomozygous116760365
103772979237729793CT20GENIChomozygous116760367
103773017837730179TA17GENIChomozygous116760369
103773035037730351AC18GENIChomozygous116562911
103773052537730526TC16GENIChomozygous116562913
103773204037732041GA15GENIChomozygous116760371
103773226437732265TC20GENIChomozygous116760373
103773228737732288GA23GENICpossibly homozygous116760375
103773472937734730AG11GENIChomozygous116760377
103773512737735128GA26GENIChomozygous116760379
103773530137735302AG9GENIChomozygous116562929
103773577137735772GA23GENIChomozygous116760381
103773643137736432AG15GENIChomozygous116760383
103773666637736667TC19GENIChomozygous116760385
103773686237736863TC20GENIChomozygous116760387
103773702837737029GT15GENIChomozygous116760389
103773791937737920CT15GENIChomozygous116760391
103773847637738477AG11GENIChomozygous116562933
103773852237738523TC13GENIChomozygous116760393
103773853237738533TC14GENIChomozygous116760395
103773886937738870TC12GENIChomozygous116760397
103774022637740227GA13GENIChomozygous116760399
103774146137741462AG11GENIChomozygous116977158
103774211937742120GT19GENIChomozygous116760401
103774300637743007TC18GENIChomozygous116760403
103774314637743147TC14GENIChomozygous116562937
103774318637743187CT18GENIChomozygous117076544
103774455537744556TC18GENIChomozygous116760405
103774558337745584TC2GENIChomozygous116760409
103774634237746343GA6GENIChomozygous116760411
103774697437746975GA13GENIChomozygous116760413
103774756137747562GC21GENIChomozygous116562941
103774902037749021CT13GENIChomozygous116760415
103774967237749673AG13GENIChomozygous116760417
103775077437750775CT15GENIChomozygous116760423