chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137969684579696846TG21GENICheterozygous50106988
137969721379697214GA15GENICheterozygous50106990
137969740579697406AG15GENICheterozygous50106992
137970369879703699TC25GENICheterozygous50106996
137970485279704853CA10GENICheterozygous50106998
137970715379707154CT9GENICheterozygous50107000
137970823379708237AACC----30GENICheterozygous50107006
137970842279708423CT15GENICheterozygous50107008
137970842379708424AG15GENICheterozygous50107010
137970846879708469CA20GENICheterozygous50107012
137970847879708479AC20GENICheterozygous50107014
137970858179708582AG28GENICheterozygous50107016
137970772179707722GT18GENICheterozygous49832463
137970772379707727TAAC----18GENICheterozygous49832464
137970988479709885A-10GENICheterozygous50107018
137970997879709979AG13GENICheterozygous50107020
137971014379710144AG19GENICheterozygous50107022
137971066779710668TC21GENICheterozygous50107024
137971086379710864AG13GENICheterozygous50107026
137971221379712214AG23GENICheterozygous50107030
137971293679712937TC16GENICheterozygous50107032
137971440279714403CT19GENICheterozygous50107034
137971494279714943GA16GENICheterozygous50107036
137971497779714978TC13GENICheterozygous50107038
137971499879715012TGTGTGTGTGTATG--------------12GENICheterozygous50107040
137971664579716646C-7GENICheterozygous51253560
137971628279716283CA15GENICheterozygous50107044