chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129888083129888128CAGAGGAAAGCAATGGGACTCACCCACATCCCCTTCTCTCACCCA37GENIChomozygous137983646
7129889121129889122GA49GENIChomozygous138223395
7129892144129892145GA42GENIChomozygous138223396
7129892719129892720TA66GENIChomozygous138223397
7129893015129893016GA53GENIChomozygous138223398
7129894506129894507AG58GENIChomozygous138223399
7129895078129895078AGGTGGGAGAGGATTAACGCAAATAAATAAA44GENIChomozygous137983647
7129895404129895405TG46GENICpossibly homozygous138223400
7129898400129898401AC23GENIChomozygous138223401
7129898463129898464TA14GENIChomozygous138223402
7129899402129899403CT36GENIChomozygous138223403
7129900701129900702GC56GENIChomozygous138223404
7129900918129900919TC59GENIChomozygous138223405
7129902390129902397TGTCCAA59GENIChomozygous137983648
7129902932129902933GA36GENIChomozygous138223406
7129903280129903281AG48GENIChomozygous138223407
7129903580129903581GT39GENIChomozygous138223408
7129904684129904685AG53GENIChomozygous138223409
7129896041129896042G33GENICheterozygous403227019
7129896041129896042GC33GENICheterozygous403227020
7129905246129905247GA57GENIChomozygous138223410
7129906202129906203GC31GENIChomozygous138223411
7129907110129907111CT48GENIChomozygous138223412
7129907385129907386GA36GENIChomozygous138223413
7129907431129907431A27GENICpossibly homozygous137983649
7129909275129909276G57GENIChomozygous137983650
7129909720129909720TACA48GENIChomozygous137983651
7129909992129909993CT56GENIChomozygous138223414
7129910029129910030TC59GENIChomozygous138223415
7129910436129910437TG34GENIChomozygous138223417
7129910295129910296GT46GENIChomozygous138223416