chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147020801870208019TC23GENIChomozygous49124417
147020856470208565TC23GENIChomozygous49124419
147021046970210470T-12GENICheterozygous49124420
147021051170210512TC29GENIChomozygous49124422
147021091670210917GGT33GENIChomozygous49124423
147021095870210959CT29GENIChomozygous49124425
147021167370211674CT28GENIChomozygous49124427
147021247170212472AC21GENIChomozygous49124429
147021254170212542TC25GENIChomozygous49124431
147021256870212569TG21GENIChomozygous49124433
147021289370212894TA37GENIChomozygous49124435
147021392070213921CT30GENICpossibly homozygous49124437
147021399370213994CT42GENIChomozygous49124439
147021485670214857TC17GENIChomozygous49124441
147021546970215470TG14GENIChomozygous49124443
147021548770215496TTGGTACAT---------10GENIChomozygous49124444
147021575670215757GA20GENIChomozygous49124446
147021601870216019CT35GENIChomozygous49124448
147021629670216297GA24GENIChomozygous49124450
147021633370216334CT24GENIChomozygous49124452
147021690470216905GC22GENIChomozygous49124454
147021718270217183GT21GENIChomozygous49124456
147021785370217854GA13GENIChomozygous49124457
147021823670218237AG14GENIChomozygous49124459
147021854770218557TGTGTGTGTG----------5GENIChomozygous49124461
147021856470218565GA17GENICheterozygous49124463
147021861670218617GA17GENIChomozygous49124465
147021881070218811GA22GENICpossibly homozygous49124467
147021896270218963CT25GENIChomozygous49124469
147021900970219010AG25GENIChomozygous49124471
147021908370219084CT25GENIChomozygous49124473
147021927770219278AC13GENIChomozygous49124475
147021979470219795CT29GENIChomozygous49124477
147021990870219909AG22GENIChomozygous49124479
147022014170220142AG20GENIChomozygous49124481
147022028770220288TC10GENIChomozygous49124483
147022036570220366TTC13GENIChomozygous49124485
147022040970220410GC19GENIChomozygous49124487
147022096470220965AG16GENIChomozygous49124489