chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17933666079336661CG7GENIChomozygous62685506
17934122879341229GA12GENICpossibly homozygous61880201
17934354079343541CT7GENIChomozygous61880202
17934357679343577TG10GENIChomozygous61880203
17934360979343610TC5GENICheterozygous61880204
17934415679344157GGAACCCC5GENIChomozygous61880205
17934427879344279AG10GENICpossibly homozygous61443911
17934471979344720C-24GENICheterozygous61880206
17934485979344860CT16GENIChomozygous61443912
17934489179344903AAACTCCTCCTC------------4GENIChomozygous61880207
17934539879345399CT16GENICheterozygous61880208
17934550879345520TCCATCCATCCA------------4GENICheterozygous61880209
17934600979346010C-6GENIChomozygous61880211
17934634679346347GA7GENICpossibly homozygous61880213
17934663979346640AG11GENICheterozygous61880214
17934706779347068CT13GENIChomozygous62685507
17934724379347244TC18GENIChomozygous62134205
17935053379350534AC9GENICheterozygous61880229
17935244279352443CCA9GENICpossibly homozygous60746013
17935374779353748GA5GENIChomozygous62685509
17935692879356929GA5GENICheterozygous62685510
17936011379360114GA12GENICheterozygous62685511
17936675979366760GA12GENICheterozygous62685512
17936773579367736GA14GENIChomozygous62685513
17937011279370113T-4GENICheterozygous61443979
17937360079373601AG17GENICpossibly homozygous61443992
17937551479375515CCTGA3GENIChomozygous60746018
17937736579377366A-19GENIChomozygous60746019