chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137969684579696846TG27GENIChomozygous50106988
137969721379697214GA12GENIChomozygous50106990
137969740579697406AG7GENIChomozygous50106992
137970369879703699TC16GENIChomozygous50106996
137970485279704853CA21GENIChomozygous50106998
137970492579704926CCTGTGTGTGTG8GENICpossibly homozygous50582816
137970492579704926CCTGTGTGTG8GENICheterozygous50524636
137970715379707154CT21GENIChomozygous50107000
137970719579707196CCATGGTGT30GENIChomozygous50107002
137970737779707378A-24GENIChomozygous50107004
137970772179707722GT23GENIChomozygous49832463
137970772379707727TAAC----23GENIChomozygous49832464
137970823379708237AACC----14GENIChomozygous50107006
137970842279708423CT27GENIChomozygous50107008
137970842379708424AG26GENIChomozygous50107010
137970846879708469CA26GENIChomozygous50107012
137970847879708479AC29GENIChomozygous50107014
137970858179708582AG18GENIChomozygous50107016
137970988479709885A-13GENIChomozygous50107018
137970997879709979AG13GENIChomozygous50107020
137971014379710144AG14GENIChomozygous50107022
137971066779710668TC20GENIChomozygous50107024
137971086379710864AG26GENIChomozygous50107026
137971125879711272ACACACACACACAC--------------1GENIChomozygous50107028
137971130379711304CG11GENIChomozygous49832466
137971221379712214AG39GENIChomozygous50107030
137971293679712937TC15GENIChomozygous50107032
137971440279714403CT30GENIChomozygous50107034
137971494279714943GA24GENIChomozygous50107036
137971497779714978TC25GENIChomozygous50107038
137971499879715014TGTGTGTGTGTATGTG----------------5GENICheterozygous50582817
137971500079715014TGTGTGTGTATGTG--------------5GENICheterozygous50582818
137971628279716283CA15GENIChomozygous50107044
137971664679716647C-4GENIChomozygous49832468