chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5167982484167982485AC15GENIChomozygous114284357
5167982709167982710TC25GENIChomozygous114284359
5167983204167983205CA32GENIChomozygous114284361
5167983558167983559AT31GENIChomozygous114284363
5167983797167983798CT29GENIChomozygous114284365
5167984086167984087AG34GENICpossibly homozygous114284367
5167984569167984570CT41GENIChomozygous114284369
5167986198167986199TA24GENIChomozygous114082915
5167983546167983547AC35GENIChomozygous114082910
5167983579167983580CG37GENIChomozygous114082912
5167984910167984911TA19GENIChomozygous114082913
5167986860167986861CT35GENIChomozygous114284371
5167986869167986870AC31GENIChomozygous114082916
5167987088167987089GA35GENIChomozygous114284373
5167987092167987093CG35GENICpossibly homozygous114284375
5167987139167987140GA37GENIChomozygous114284377
5167987656167987657CA33GENIChomozygous114284379
5167987707167987708CT28GENIChomozygous114284381
5167987852167987853CT25GENIChomozygous114284383
5167988092167988093AC35GENIChomozygous114284385
5167988795167988796GA40GENIChomozygous114284387
5167989472167989473GC31GENIChomozygous114284389
5167990144167990145TC22GENIChomozygous114284391
5167990241167990242TA22GENIChomozygous114284393
5167990590167990591TC46GENIChomozygous114082922
5167991620167991621AG19GENIChomozygous114082923
5167995107167995108CT33GENIChomozygous114082929
5167995371167995372TC27GENIChomozygous114082931
5167995418167995419TC29GENIChomozygous114082932
5167996440167996441CT27GENIChomozygous114284395
5167999302167999303GA21GENIChomozygous114082936
5167999633167999634AT20GENIChomozygous114284397
5168000088168000089TC39GENIChomozygous114284399
5168000697168000698CT25GENIChomozygous114284401