chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109666462109666463CA11GENIChomozygous116909638
10109666970109666971CT12GENIChomozygous116909639
10109667230109667231CG15GENIChomozygous116909640
10109667347109667348CT15GENIChomozygous116909641
10109667406109667407AG15GENIChomozygous116718989
10109667516109667517GT19GENIChomozygous116909642
10109667691109667692CG12GENIChomozygous116909643
10109667928109667929CT17GENIChomozygous116909644
10109668173109668174GA15GENIChomozygous116909645
10109668501109668502TC13GENIChomozygous116909646
10109668514109668515TC11GENIChomozygous116909647
10109668573109668574GA14GENIChomozygous116909648
10109668678109668679TG14GENIChomozygous116909649
10109669026109669027CT17GENIChomozygous116909650
10109669235109669236TC9GENIChomozygous116909651
10109669365109669366CT12GENIChomozygous116909652
10109669824109669825CG13GENIChomozygous116909653
10109669839109669840CT14GENIChomozygous116909654
10109669857109669858GA15GENIChomozygous116909655
10109670591109670592CT12GENIChomozygous116909656
10109670696109670697AG12GENIChomozygous116909657
10109670836109670837AG17GENIChomozygous116909658
10109671091109671092CA18GENIChomozygous116909659
10109671163109671164GA15GENIChomozygous116909660
10109671846109671847CT7GENIChomozygous116909661
10109671847109671848AG8GENIChomozygous116909662
10109672229109672230TC12GENIChomozygous116909663
10109672473109672474CT19GENIChomozygous116718993
10109672584109672585GA15GENIChomozygous116909664
10109672743109672744GC20GENIChomozygous116909665
10109673077109673078AG13GENIChomozygous116909666
10109673412109673413AG17GENIChomozygous116909667
10109674110109674111AG15GENIChomozygous116718995
10109673548109673549TG13GENIChomozygous116909668
10109673790109673791AG15GENIChomozygous116909669
10109673838109673839AG13GENIChomozygous116909670
10109674118109674118G14GENIChomozygous128860702
10109667624109667624CAT15GENIChomozygous132148012
10109670026109670027C14GENIChomozygous132148013
10109670171109670171GT11GENIChomozygous132148014