| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:223957243-223957494 | Common:4; Rare:96 | ||||
| chr2:224585506-224585906 | Common:2; Rare:101 | ||||
| chr2:224982377-224982528 | Rare:15 | ||||
| chr2:225400315-225400470 | Rare:26 | ||||
| chr2:226835861-226836146 | Common:1; Rare:118 | ||||
| chr2:227325123-227325426 | Common:6; Rare:118 | ||||
| chr2:227718010-227718118 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr2:229921269-229921471 | Common:3; Rare:48 | ||||
| chr2:229921904-229922513 | Common:4; Rare:210 | ||||
| chr2:229923167-229923228 | Rare:17 | ||||
| chr2:229923229-229923265 | Common:1; Rare:9 | ||||
| chr2:231056562-231057028 | Common:4; Rare:134 | ||||
| chr2:231198489-231198753 | Common:1; Rare:86 | ||||
| chr2:231270742-231271009 | Common:1; Rare:63 | ||||
| chr2:231460160-231460566 | Common:1; Rare:143 |