| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10448122-10448251 | Rare:30 | ||||
| chr2:10448391-10448749 | Common:1; Rare:115 | ||||
| chr2:10689919-10690024 | Common:2; Rare:35 | ||||
| chr2:11746475-11746655 | Common:1; Rare:55; Clinvar:2 | ||||
| chr2:12716753-12717075 | Common:1; Rare:91 | ||||
| chr2:17540354-17540735 | Common:2; Rare:98 | ||||
| chr2:17753689-17754159 | Common:4; Rare:147; Clinvar (benign):1 | ||||
| chr2:19901652-19902051 | Common:2; Rare:160 | ||||
| chr2:19990055-19990211 | Rare:40 | ||||
| chr2:20051500-20051845 | Common:1; Rare:99 | ||||
| chr2:20225356-20225481 | Common:1; Rare:41 | ||||
| chr2:20350822-20351034 | Common:1; Rare:86 | ||||
| chr2:20446833-20447116 | Common:4; Rare:124 | ||||
| chr2:20447280-20447505 | Common:2; Rare:78 | ||||
| chr2:20447510-20448216 | Common:1; Rare:205 |