chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1142061248142061249CA25GENIChomozygous60875090
1142061348142061352CACA----6GENICheterozygous60875091
1142061350142061352CA--6GENICheterozygous60875092
1142063333142063334AC24GENIChomozygous60875093
1142064186142064187GGA11GENICheterozygous61673656
1142064219142064220A-9GENICpossibly homozygous60875094
1142064281142064282CA9GENIChomozygous60875095
1142064501142064502AC8GENIChomozygous60875096
1142064556142064558TT--11GENIChomozygous60875097
1142065013142065025AAGGAAGGAAGG------------10GENIChomozygous62269376
1142065138142065139GA24GENIChomozygous60875100
1142065834142065835AATGGCCTTGTTGGAGTGGGTG5GENIChomozygous62161774
1142066040142066041G-9GENIChomozygous60875104
1142066386142066387TC17GENIChomozygous60875105
1142066630142066631AG19GENIChomozygous60875106
1142066812142066813CCA22GENIChomozygous60875107
1142067469142067473ACAC----2GENICheterozygous62312887
1142067471142067473AC--2GENICheterozygous62269377
1142068264142068265GA17GENIChomozygous60875109
1142068894142068895TTCCCCCCCC10GENICheterozygous62269378
1142068896142068897TTCTCTCTCTCTCTTTCTCTCTCC11GENICheterozygous62246571
1142069447142069448CT24GENIChomozygous60875115
1142069620142069621CCTTTTTTTTT1GENIChomozygous62161782
1142070207142070208CT13GENIChomozygous60875116
1142071335142071336T-14GENIChomozygous60875117
1142072251142072252AAAAC18GENIChomozygous60875119