| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:182866556-182866733 | Common:1; Rare:43 | ||||
| chr2:183037996-183038072 | Rare:21 | ||||
| chr2:183078680-183078803 | Rare:24 | ||||
| chr2:183124252-183124452 | Common:4; Rare:67 | ||||
| chr2:186485977-186486348 | Common:3; Rare:101 | ||||
| chr2:186589589-186589846 | Rare:57 | ||||
| chr2:186589988-186590355 | Rare:109 | ||||
| chr2:188292706-188292849 | Rare:35 | ||||
| chr2:188974218-188974568 | Rare:89; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189441094-189441511 | Common:2; Rare:127 | ||||
| chr2:189580742-189580938 | Common:1; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783956-189784111 | Common:3; Rare:54; Clinvar (benign):1 | ||||
| chr2:189784275-189784558 | Common:4; Rare:99; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343941-190344051 | Rare:23 | ||||
| chr2:190534631-190534908 | Common:2; Rare:83 |