chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98011847780118478AG72GENIChomozygous117580515
98011851580118516GA74GENIChomozygous117848207
98011858480118585GC62GENIChomozygous117848208
98011893980118940AG50GENIChomozygous117848209
98011926280119263TC53GENIChomozygous117594100
98011928980119290GA53GENIChomozygous117580521
98012033180120332CT36GENIChomozygous117580525
98012116280121163AG43GENIChomozygous117848210
98012276380122764AG53GENIChomozygous117580549
98012282180122822CG61GENIChomozygous117580551
98012324180123242CG40GENIChomozygous117848211
98012325380123254GC41GENIChomozygous117580555
98012439080124391GA59GENIChomozygous117848212
98012466180124662AG60GENIChomozygous117848213
98012481980124820TC69GENIChomozygous117848214
98011987480119875T52GENIChomozygous133210820
98012329080123290TTTC42GENIChomozygous133210821
98012388380123884CT69GENIChomozygous120269971
98012662680126627AG51GENIChomozygous117879319
98012557880125578A50GENIChomozygous128727203
98012754380127544TC40GENIChomozygous117879323
98012996980129970CT52GENIChomozygous120269972
98013004880130049AC58GENIChomozygous120269973
98013021880130219CA48GENIChomozygous117879325
98013253780132538TG54GENIChomozygous117879331
98013270780132708AG58GENIChomozygous117879333
98013409580134096CT38GENICpossibly homozygous120269974
98013436980134370CT33GENIChomozygous117879339
98013452580134526CT20GENIChomozygous120450001
98013452780134528CT20GENIChomozygous120450003
98013460580134606AG40GENIChomozygous117879343
98013473180134732AG45GENIChomozygous117879345
98013504380135044AG55GENIChomozygous117879347
98013552580135526CG56GENIChomozygous117879349
98013622280136223TA51GENIChomozygous117848229
98013667380136674CT60GENIChomozygous120269975
98013703580137036GA68GENIChomozygous120269976
98013840380138404CT41GENIChomozygous120269977
98013874880138749GA44GENIChomozygous120269978
98013925480139255AG55GENIChomozygous120269979
98013969480139701GTTTTTT45GENIChomozygous133210828
98014012180140121T51GENICpossibly homozygous133210829
98014061080140611AG60GENIChomozygous120269980
98014073980140740CT49GENIChomozygous120269981
98014091680140917CT61GENIChomozygous120269982
98014125680141257AG47GENIChomozygous120269983
98014141380141414CT46GENIChomozygous120269984
98014185680141857CA49GENICpossibly homozygous120269985
98014200480142005CT66GENIChomozygous120269986
98014207780142078AT72GENIChomozygous120269987
98014225980142260CT62GENIChomozygous120269988
98014254580142546CT62GENIChomozygous120269989
98014272780142728AG40GENIChomozygous117879361
98014280080142801GT47GENIChomozygous120269990
98014283780142838GA47GENIChomozygous120269991
98014286780142868TC49GENIChomozygous117879365
98014300180143002TC35GENIChomozygous120269992
98014306380143064AC40GENIChomozygous120269993
98014312180143122CT53GENIChomozygous120269994
98014322580143226CT58GENIChomozygous120269995
98014346080143460GTCTGTCTGTCTTTGCT40GENIChomozygous131071625
98012750680127509AAG31GENIChomozygous133419370
98013432980134329C14GENIChomozygous133419371
98012766080127660CTCACACA32GENIChomozygous131071622
98013391080133925TATGCAAATGTTTCT42GENIChomozygous131071623
98014138380141387AAAA47GENIChomozygous131071624
98014381280143813GT52GENIChomozygous120269996
98014390480143905GA47GENIChomozygous120269997
98014423680144237A56GENICpossibly homozygous131071626
98014438780144388TC61GENIChomozygous120269998
98014447380144474CT51GENIChomozygous120269999