chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129888083129888128CAGAGGAAAGCAATGGGACTCACCCACATCCCCTTCTCTCACCCA11GENIChomozygous137983646
7129893015129893016GA17GENIChomozygous138223398
7129889121129889122GA9GENIChomozygous138223395
7129892144129892145GA21GENIChomozygous138223396
7129892719129892720TA18GENIChomozygous138223397
7129894506129894507AG16GENIChomozygous138223399
7129895078129895078AGGTGGGAGAGGATTAACGCAAATAAATAAA11GENIChomozygous137983647
7129895404129895405TG15GENIChomozygous138223400
7129898400129898401AC6GENIChomozygous138223401
7129898463129898464TA4GENIChomozygous138223402
7129899402129899403CT14GENIChomozygous138223403
7129900701129900702GC24GENIChomozygous138223404
7129900918129900919TC17GENIChomozygous138223405
7129902390129902397TGTCCAA19GENIChomozygous137983648
7129902932129902933GA18GENIChomozygous138223406
7129903280129903281AG18GENIChomozygous138223407
7129903580129903581GT15GENIChomozygous138223408
7129904684129904685AG28GENIChomozygous138223409
7129905246129905247GA20GENIChomozygous138223410
7129906202129906203GC12GENIChomozygous138223411
7129907110129907111CT14GENIChomozygous138223412
7129907385129907386GA12GENIChomozygous138223413
7129907431129907431A13GENICheterozygous137983649
7129909275129909276G28GENIChomozygous137983650
7129909720129909720TACA18GENIChomozygous137983651
7129909992129909993CT12GENIChomozygous138223414
7129910029129910030TC17GENIChomozygous138223415
7129910295129910296GT15GENIChomozygous138223416
7129910436129910437TG11GENIChomozygous138223417
7129896041129896042GC13GENICheterozygous403227020
7129896041129896042G13GENICheterozygous403227019