Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:227548956-227549003 | Rare:9 | ||||
chr2:227553499-227553772 | Common:1; Rare:60 | ||||
chr2:229771498-229771538 | Rare:8; Clinvar (pathogenic):1 | ||||
chr2:229830758-229830942 | Rare:39 | ||||
chr2:229831475-229831654 | Rare:38 | ||||
chr2:229833257-229833278 | Rare:4 | ||||
chr2:230469829-230470096 | Common:2; Rare:69 | ||||
chr2:230794129-230794303 | Common:2; Rare:39 | ||||
chr2:230809590-230809873 | Common:1; Rare:57 | ||||
chr2:230877167-230877404 | Rare:72 | ||||
chr2:231161324-231161348 | Rare:3 | ||||
chr2:231161352-231161756 | Rare:74 | ||||
chr2:231455223-231455626 | Common:1; Rare:145 | ||||
chr2:231712395-231712864 | Common:3; Rare:142 | ||||
chr2:232562554-232562746 | Rare:33 |