chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121351511121351512AC24GENIChomozygous955429407
7121351659121351660AG29GENIChomozygous955429408
7121351666121351667GA27GENIChomozygous955429409
7121352112121352113AG30GENIChomozygous955429410
7121352821121352822AG22GENIChomozygous955429411
7121354414121354415CT26GENIChomozygous955429412
7121354892121354893AC19GENIChomozygous955429413
7121355447121355448TA15GENICpossibly homozygous955429414
7121356568121356569GA31GENIChomozygous955429415
7121357005121357006TG26GENIChomozygous955429416
7121364825121364826GA24GENIChomozygous955429417
7121367352121367353TC29GENIChomozygous955429418
7121369373121369374AG35GENIChomozygous955429419
7121369747121369748CT46GENIChomozygous955429420
7121369953121369954GA39GENIChomozygous955429421
7121370431121370432TC35GENIChomozygous955429422
7121370678121370679CT28GENIChomozygous955429423
7121370951121370952GT33GENIChomozygous955429424
7121372869121372870TC29GENIChomozygous955429425
7121373043121373044TC21GENIChomozygous955429426
7121373775121373776GA25GENIChomozygous955429427
7121374131121374132AG42GENIChomozygous955429428
7121374460121374461GA22GENIChomozygous955429429
7121374767121374768CT43GENIChomozygous955429430
7121374815121374816CA32GENICpossibly homozygous955429431
7121375655121375656TC17GENIChomozygous955429432
7121376233121376234TC22GENIChomozygous955429433
7121378332121378333TC37GENIChomozygous955429434
7121381943121381944TC27GENIChomozygous955429435