chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224869251224869253GT39GENICpossibly homozygous130833526
1224869722224869723G17GENIChomozygous130833527
1224870020224870021TC46GENIChomozygous120595278
1224871105224871106GA35GENIChomozygous120595280
1224874997224874998GT21GENIChomozygous108556255
1224874539224874540TC37GENIChomozygous108556253
1224874566224874567TC32GENIChomozygous108556254
1224875195224875196AG50GENIChomozygous108556258
1224877918224877919TC47GENIChomozygous108556260
1224878076224878077AG56GENIChomozygous108556261
1224878084224878085GA57GENIChomozygous108556262
1224878150224878151GA50GENIChomozygous120595282
1224879567224879568AC45GENIChomozygous120595284
1224880084224880085GA44GENIChomozygous108996799
1224881026224881027AG43GENIChomozygous108556265
1224881341224881342TC49GENIChomozygous108556266
1224882153224882154AG47GENIChomozygous108996800
1224882180224882181TC44GENIChomozygous108996801
1224884627224884627AAATAT45GENIChomozygous130833528
1224875027224875028AG19GENIChomozygous131797290
1224879809224879809TGTG24GENIChomozygous127487419
1224875923224875924GA25GENIChomozygous130853152