| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208255014-208255238 | Common:2; Rare:58 | ||||
| chr2:208266121-208266376 | Common:6; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210170727-210170878 | Rare:64 | ||||
| chr2:210477572-210477690 | Rare:39 | ||||
| chr2:215312031-215312139 | Common:7; Rare:50 | ||||
| chr2:215435648-215436166 | Common:3; Rare:129 | ||||
| chr2:216081761-216081906 | Common:1; Rare:47 | ||||
| chr2:216498740-216498877 | Common:5; Rare:54 | ||||
| chr2:216694438-216694854 | Rare:101 | ||||
| chr2:216695359-216695688 | Rare:62 | ||||
| chr2:217901881-217902167 | Common:3; Rare:47 | ||||
| chr2:217905399-217905647 | Rare:49 | ||||
| chr2:217937114-217937200 | Common:2; Rare:11 | ||||
| chr2:217937253-217937297 | Rare:11 | ||||
| chr2:217978622-217978713 | Rare:25 |