chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147020801870208019TC24GENIChomozygous49124417
147020856470208565TC31GENIChomozygous49124419
147021046970210470T-10GENIChomozygous49124420
147021051170210512TC15GENIChomozygous49124422
147021091670210917GGT6GENIChomozygous49124423
147021095870210959CT8GENIChomozygous49124425
147021167370211674CT29GENIChomozygous49124427
147021247170212472AC31GENIChomozygous49124429
147021254170212542TC38GENIChomozygous49124431
147021256870212569TG35GENIChomozygous49124433
147021289370212894TA17GENIChomozygous49124435
147021392070213921CT15GENIChomozygous49124437
147021399370213994CT16GENIChomozygous49124439
147021485670214857TC31GENIChomozygous49124441
147021546970215470TG20GENIChomozygous49124443
147021548770215496TTGGTACAT---------10GENIChomozygous49124444
147021575670215757GA23GENIChomozygous49124446
147021601870216019CT27GENIChomozygous49124448
147021629670216297GA40GENIChomozygous49124450
147021633370216334CT40GENIChomozygous49124452
147021690470216905GC42GENIChomozygous49124454
147021718270217183GT30GENIChomozygous49124456
147021785370217854GA21GENIChomozygous49124457
147021823670218237AG20GENIChomozygous49124459
147021854770218557TGTGTGTGTG----------6GENIChomozygous49124461
147021856470218565GA19GENICheterozygous49124463
147021861670218617GA25GENICpossibly homozygous49124465
147021881070218811GA34GENIChomozygous49124467
147021896270218963CT20GENIChomozygous49124469
147021900970219010AG13GENIChomozygous49124471
147021908370219084CT13GENIChomozygous49124473
147021927770219278AC28GENIChomozygous49124475
147021979470219795CT28GENIChomozygous49124477
147021990870219909AG19GENIChomozygous49124479
147022014170220142AG13GENIChomozygous49124481
147022028770220288TC18GENIChomozygous49124483
147022036570220366TTC23GENIChomozygous49124485
147022040970220410GC31GENIChomozygous49124487
147022096470220965AG32GENIChomozygous49124489