chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129888083129888128CAGAGGAAAGCAATGGGACTCACCCACATCCCCTTCTCTCACCCA10GENIChomozygous137983646
7129889121129889122GA24GENIChomozygous138223395
7129892144129892145GA26GENIChomozygous138223396
7129892719129892720TA19GENIChomozygous138223397
7129893015129893016GA22GENIChomozygous138223398
7129894506129894507AG19GENIChomozygous138223399
7129895078129895078AGGTGGGAGAGGATTAACGCAAATAAATAAA17GENIChomozygous137983647
7129895404129895405TG29GENIChomozygous138223400
7129898400129898401AC15GENIChomozygous138223401
7129898463129898464TA9GENIChomozygous138223402
7129899402129899403CT14GENIChomozygous138223403
7129900701129900702GC22GENIChomozygous138223404
7129900918129900919TC29GENIChomozygous138223405
7129902390129902397TGTCCAA21GENIChomozygous137983648
7129902932129902933GA6GENIChomozygous138223406
7129903280129903281AG20GENIChomozygous138223407
7129903580129903581GT12GENIChomozygous138223408
7129904684129904685AG12GENIChomozygous138223409
7129905246129905247GA28GENIChomozygous138223410
7129906202129906203GC13GENIChomozygous138223411
7129907110129907111CT14GENIChomozygous138223412
7129907385129907386GA7GENIChomozygous138223413
7129907431129907431A7GENIChomozygous137983649
7129909275129909276G16GENIChomozygous137983650
7129909720129909720TACA13GENIChomozygous137983651
7129909992129909993CT20GENIChomozygous138223414
7129910029129910030TC21GENIChomozygous138223415
7129910295129910296GT15GENIChomozygous138223416
7129910436129910437TG13GENIChomozygous138223417