| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219543756-219544077 | Common:3; Rare:99 | ||||
| chr2:219597737-219597884 | Common:1; Rare:50 | ||||
| chr2:221572244-221572528 | Common:6; Rare:99 | ||||
| chr2:222656027-222656433 | Common:3; Rare:129 | ||||
| chr2:223602296-223602451 | Rare:44 | ||||
| chr2:223957301-223957495 | Common:3; Rare:78 | ||||
| chr2:224039101-224039179 | Rare:18 | ||||
| chr2:224039282-224039428 | Rare:53 | ||||
| chr2:227325184-227325491 | Common:6; Rare:106 | ||||
| chr2:227718010-227718118 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr2:229921899-229922524 | Common:4; Rare:222 | ||||
| chr2:230219951-230220001 | Rare:6 | ||||
| chr2:230416119-230416231 | Rare:35 | ||||
| chr2:231198436-231198717 | Common:2; Rare:97 | ||||
| chr2:231464142-231464215 | Rare:20 |