| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10406042-10406189 | Common:2; Rare:21 | ||||
| chr2:10443229-10443570 | Rare:96 | ||||
| chr2:10602804-10603083 | Common:2; Rare:69 | ||||
| chr2:10662995-10663082 | Rare:26 | ||||
| chr2:10668657-10668999 | Common:2; Rare:75 | ||||
| chr2:11102764-11102962 | Rare:35 | ||||
| chr2:11804998-11805157 | Rare:46; Clinvar (benign):1 | ||||
| chr2:15628754-15628849 | Rare:24 | ||||
| chr2:17592800-17592919 | Common:2; Rare:22 | ||||
| chr2:18560144-18560178 | Rare:10 | ||||
| chr2:18577470-18577628 | Common:2; Rare:25 | ||||
| chr2:18947925-18948018 | Common:1; Rare:16 | ||||
| chr2:19348006-19348102 | Common:1; Rare:40 | ||||
| chr2:20037313-20037641 | Rare:93 | ||||
| chr2:20207734-20207875 | Common:1; Rare:28 |