chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137969684579696846TG31GENIChomozygous50106988
137969721379697214GA22GENIChomozygous50106990
137969740579697406AG7GENIChomozygous50106992
137969745479697455TTA1GENIChomozygous50524634
137969745779697458TTATTTATGTA1GENIChomozygous50524635
137970369879703699TC13GENIChomozygous50106996
137970485279704853CA28GENIChomozygous50106998
137970492579704926CCTGTGTGTG4GENIChomozygous50524636
137970715379707154CT20GENIChomozygous50107000
137970719579707196CCATGGTGT14GENIChomozygous50107002
137970737779707378A-21GENIChomozygous50107004
137970823379708237AACC----19GENIChomozygous50107006
137970842279708423CT13GENIChomozygous50107008
137970842379708424AG13GENIChomozygous50107010
137970846879708469CA8GENIChomozygous50107012
137970847879708479AC8GENIChomozygous50107014
137970858179708582AG21GENIChomozygous50107016
137970988479709885A-18GENIChomozygous50107018
137970997879709979AG27GENIChomozygous50107020
137971014379710144AG20GENIChomozygous50107022
137971066779710668TC22GENIChomozygous50107024
137971086379710864AG21GENICpossibly homozygous50107026
137971125879711272ACACACACACACAC--------------4GENIChomozygous50107028
137971221379712214AG18GENIChomozygous50107030
137971293679712937TC22GENIChomozygous50107032
137971440279714403CT21GENIChomozygous50107034
137970772179707722GT17GENIChomozygous49832463
137970772379707727TAAC----17GENIChomozygous49832464
137971130379711304CG9GENIChomozygous49832466
137971446079714461TA16GENIChomozygous50436775
137971494279714943GA9GENIChomozygous50107036
137971497779714978TC11GENIChomozygous50107038
137971628279716283CA22GENIChomozygous50107044
137971664579716647CC--7GENICheterozygous49959729
137971664679716647C-7GENICpossibly homozygous49832468