| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177212400-177212821 | Common:5; Rare:173 | ||||
| chr2:177263408-177263551 | Rare:33 | ||||
| chr2:177264630-177264863 | Common:2; Rare:76 | ||||
| chr2:177392669-177393059 | Common:2; Rare:137; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:178451090-178451378 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:181891665-181892010 | Common:4; Rare:138 | ||||
| chr2:182716184-182716446 | Common:1; Rare:86 | ||||
| chr2:183124252-183124452 | Common:4; Rare:67 | ||||
| chr2:186485994-186486360 | Common:3; Rare:106 | ||||
| chr2:186590109-186590335 | Rare:69 | ||||
| chr2:189441133-189441511 | Common:2; Rare:116 | ||||
| chr2:189674443-189674542 | Common:1; Rare:25 | ||||
| chr2:189784275-189784537 | Common:4; Rare:94; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190534696-190534925 | Common:1; Rare:73 |