| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:149587275-149587397 | Common:1; Rare:27 | ||||
| chr2:149587672-149587892 | Common:1; Rare:63; Clinvar:1 | ||||
| chr2:151289609-151289759 | Common:1; Rare:35 | ||||
| chr2:151409770-151410170 | Common:3; Rare:136 | ||||
| chr2:151828287-151828535 | Common:2; Rare:80 | ||||
| chr2:152098686-152099160 | Common:1; Rare:161; Clinvar:6; Clinvar (benign):6 | ||||
| chr2:152175670-152176092 | Common:3; Rare:117 | ||||
| chr2:152717806-152718048 | Rare:90 | ||||
| chr2:152718450-152718718 | Rare:116 | ||||
| chr2:156435582-156435664 | Common:1; Rare:18 | ||||
| chr2:156436063-156436459 | Common:3; Rare:110 | ||||
| chr2:156473507-156473599 | Rare:15 | ||||
| chr2:158456649-158456908 | Common:1; Rare:87 | ||||
| chr2:158968487-158968702 | Rare:69 | ||||
| chr2:159286638-159286900 | Common:5; Rare:99 |