| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:182867163-182867242 | Rare:19 | ||||
| chr2:183078680-183078799 | Rare:23 | ||||
| chr2:183124252-183124460 | Common:4; Rare:71 | ||||
| chr2:186485983-186486370 | Common:3; Rare:112 | ||||
| chr2:186590064-186590355 | Rare:91 | ||||
| chr2:187448130-187448407 | Rare:43 | ||||
| chr2:188291639-188292088 | Common:5; Rare:127 | ||||
| chr2:188292692-188292869 | Common:1; Rare:44 | ||||
| chr2:188293007-188293064 | Rare:7 | ||||
| chr2:189441046-189441511 | Common:3; Rare:148 | ||||
| chr2:189580760-189580938 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783906-189784133 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:189784254-189784557 | Common:4; Rare:107; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:190534651-190534887 | Common:1; Rare:74 | ||||
| chr2:190648583-190648916 | Common:1; Rare:106 |