chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117518524117518525CT15GENIChomozygous118512061
7117518728117518729GA10GENIChomozygous115847417
7117520169117520170AG19GENIChomozygous115847419
7117521513117521514GC10GENIChomozygous115847421
7117521820117521821GA6GENIChomozygous115847423
7117523204117523205CT12GENIChomozygous115847427
7117526373117526374CA4GENIChomozygous126647688
7117526807117526808CA16GENIChomozygous118512062
7117526958117526959TC9GENIChomozygous115847439
7117528304117528305GA19GENIChomozygous115847441
7117529078117529079TG23GENIChomozygous115847445
7117529191117529192TC11GENIChomozygous115847447
7117529808117529809GA15GENIChomozygous115847449
7117529849117529850GT11GENIChomozygous115847451
7117530897117530898GC22GENIChomozygous118512063
7117530978117530979GA15GENIChomozygous118512064
7117533325117533326CT9GENIChomozygous118512065
7117533357117533358GA17GENIChomozygous115847453
7117533398117533399AG11GENIChomozygous118512066
7117533544117533545AG11GENIChomozygous118512067
7117537439117537440GA22GENIChomozygous115847457
7117537961117537962TA15GENIChomozygous118512068