chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129888083129888128CAGAGGAAAGCAATGGGACTCACCCACATCCCCTTCTCTCACCCA15GENIChomozygous137983646
7129893015129893016GA19GENIChomozygous138223398
7129889121129889122GA18GENIChomozygous138223395
7129892144129892145GA17GENIChomozygous138223396
7129892719129892720TA19GENIChomozygous138223397
7129894506129894507AG19GENIChomozygous138223399
7129895078129895078AGGTGGGAGAGGATTAACGCAAATAAATAAA13GENIChomozygous137983647
7129895404129895405TG29GENIChomozygous138223400
7129898400129898401AC10GENIChomozygous138223401
7129898463129898464TA7GENIChomozygous138223402
7129899402129899403CT12GENIChomozygous138223403
7129900701129900702GC19GENIChomozygous138223404
7129900918129900919TC18GENIChomozygous138223405
7129902390129902397TGTCCAA23GENIChomozygous137983648
7129902932129902933GA13GENIChomozygous138223406
7129903280129903281AG16GENIChomozygous138223407
7129903580129903581GT20GENIChomozygous138223408
7129903688129903689GA14GENIChomozygous144388458
7129904684129904685AG11GENIChomozygous138223409
7129905246129905247GA19GENIChomozygous138223410
7129906202129906203GC10GENIChomozygous138223411
7129907110129907111CT14GENIChomozygous138223412
7129907385129907386GA11GENIChomozygous138223413
7129907431129907431A10GENICheterozygous137983649
7129909275129909276G15GENIChomozygous137983650
7129909720129909720TACA14GENIChomozygous137983651
7129909992129909993CT13GENIChomozygous138223414
7129910029129910030TC14GENIChomozygous138223415
7129910295129910296GT13GENIChomozygous138223416
7129910436129910437TG11GENIChomozygous138223417
7129896041129896042GC14GENICheterozygous403227020
7129896041129896042G14GENIChomozygous403227019