| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:172474645-172474952 | Common:1; Rare:61 | ||||
| chr2:172485044-172485201 | Rare:37; Clinvar:1 | ||||
| chr2:172486986-172487372 | Common:1; Rare:108; Clinvar:2 | ||||
| chr2:172489295-172489602 | Common:1; Rare:73 | ||||
| chr2:173021474-173021527 | Rare:7 | ||||
| chr2:173457508-173457660 | Rare:31 | ||||
| chr2:174013455-174013638 | Rare:41 | ||||
| chr2:174523406-174523536 | Rare:24 | ||||
| chr2:174548010-174548244 | Common:2; Rare:56 | ||||
| chr2:174719967-174720311 | Common:4; Rare:62 | ||||
| chr2:174787922-174788026 | Rare:28 | ||||
| chr2:175257024-175257437 | Common:8; Rare:155 | ||||
| chr2:176085305-176085443 | Rare:26 | ||||
| chr2:176177813-176178187 | Common:5; Rare:108 | ||||
| chr2:176637574-176637767 | Common:4; Rare:69 |