| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231464138-231464280 | Rare:43 | ||||
| chr2:231464397-231465098 | Common:4; Rare:222 | ||||
| chr2:231706401-231706668 | Common:2; Rare:64 | ||||
| chr2:231706711-231707492 | Common:1; Rare:195 | ||||
| chr2:231707755-231707878 | Common:1; Rare:52 | ||||
| chr2:231708238-231708571 | Common:1; Rare:129 | ||||
| chr2:231709026-231709435 | Common:6; Rare:174 | ||||
| chr2:231709960-231710001 | Common:1; Rare:11 | ||||
| chr2:231710207-231710573 | Common:4; Rare:187 | ||||
| chr2:231781212-231781559 | Common:3; Rare:98 | ||||
| chr2:231781561-231781826 | Common:2; Rare:74 | ||||
| chr2:231782026-231782221 | Rare:46 | ||||
| chr2:231786173-231786681 | Common:3; Rare:143 | ||||
| chr2:231961214-231961276 | Rare:18 | ||||
| chr2:231961331-231962007 | Common:2; Rare:173; Clinvar:4 |