Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:10808894-10809154 | Common:2; Rare:109 | ||||
chr11:10858013-10858266 | Common:3; Rare:83 | ||||
chr11:11621965-11622247 | Common:4; Rare:113 | ||||
chr11:11841938-11842079 | Common:1; Rare:39 | ||||
chr11:14520269-14520510 | Rare:80 | ||||
chr11:14643591-14643821 | Common:2; Rare:86 | ||||
chr11:14644642-14644858 | Rare:96 | ||||
chr11:14891627-14891798 | Rare:51 | ||||
chr11:16738456-16738729 | Common:3; Rare:58 | ||||
chr11:16744497-16744684 | Common:1; Rare:43 | ||||
chr11:17014198-17014341 | Rare:50 | ||||
chr11:17077618-17077895 | Common:2; Rare:118 | ||||
chr11:17207905-17208078 | Common:2; Rare:69 | ||||
chr11:17276542-17276828 | Common:5; Rare:80; Clinvar:4; Clinvar (pathogenic):1 | ||||
chr11:17351680-17351811 | Rare:24 |