| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190980628-190980920 | Common:1; Rare:47 | ||||
| chr2:191169496-191170154 | Common:5; Rare:210 | ||||
| chr2:191171373-191172208 | Common:8; Rare:180 | ||||
| chr2:191219363-191219790 | Common:6; Rare:104 | ||||
| chr2:191318529-191318716 | Rare:41 | ||||
| chr2:191329911-191330112 | Rare:52 | ||||
| chr2:191358258-191358559 | Rare:55 | ||||
| chr2:191415885-191416169 | Rare:115 | ||||
| chr2:191500785-191501310 | Common:8; Rare:153 | ||||
| chr2:191544161-191545110 | Common:6; Rare:287 | ||||
| chr2:191631854-191632254 | Common:1; Rare:120 | ||||
| chr2:191758397-191759046 | Common:9; Rare:188 | ||||
| chr2:192749735-192749850 | Rare:17 | ||||
| chr2:193347092-193347795 | Common:11; Rare:208 | ||||
| chr2:193502616-193502805 | Common:5; Rare:64 |