chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167178519771785198CT17GENIChomozygous111855455
167178603871786039AG23GENIChomozygous111855457
167178633871786339CT23GENIChomozygous112077223
167178719971787200TA6GENIChomozygous112077225
167178720071787201CA6GENIChomozygous112077227
167178730571787306AG13GENIChomozygous111855458
167178740771787408AG16GENIChomozygous111855459
167178760671787607AC19GENIChomozygous111855460
167178974471789745TC34GENIChomozygous111855468
167179039071790391TC8GENIChomozygous111855469
167179598571795986CA8GENIChomozygous112263973
167179599371795994AG10GENIChomozygous111855471
167179662271796623CT17GENICpossibly homozygous112263974
167179762171797622AG12GENIChomozygous111855480
167179905971799060TA31GENICpossibly homozygous119172739
167180054771800548CT11GENIChomozygous112026995
167178860471788605TC6GENIChomozygous112277291
167179060371790604GA15GENIChomozygous112358835
167179534071795341CT11GENIChomozygous112358837
167179615571796156AG14GENIChomozygous112358839
167179692571796926CT19GENIChomozygous112358841
167179861371798614GA5GENIChomozygous112358843
167179858271798583GA13GENIChomozygous112026993
167180187971801880GA20GENIChomozygous112026997
167180240771802408TC14GENIChomozygous112358847
167180271871802719GA19GENIChomozygous111855530