| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:183124277-183124460 | Common:1; Rare:66 | ||||
| chr2:186486003-186486348 | Common:3; Rare:96 | ||||
| chr2:186590140-186590335 | Rare:57 | ||||
| chr2:186693922-186694128 | Rare:86 | ||||
| chr2:188291503-188292088 | Common:8; Rare:166 | ||||
| chr2:188292714-188292842 | Rare:34 | ||||
| chr2:188292989-188293022 | Rare:6 | ||||
| chr2:189441072-189441438 | Common:1; Rare:97 | ||||
| chr2:189783965-189784078 | Common:2; Rare:38 | ||||
| chr2:189784276-189784564 | Common:4; Rare:101; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343961-190344031 | Rare:14 | ||||
| chr2:190534702-190534853 | Common:1; Rare:50 | ||||
| chr2:191014138-191014368 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245293-191245487 | Common:1; Rare:65 | ||||
| chr2:191246159-191246314 | Common:1; Rare:44 |