| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:98730835-98731390 | Common:6; Rare:171 | ||||
| chr2:98731412-98731453 | Common:1; Rare:12 | ||||
| chr2:98869358-98869715 | Common:4; Rare:72 | ||||
| chr2:99140684-99140701 | Rare:3 | ||||
| chr2:99141099-99141780 | Common:3; Rare:247 | ||||
| chr2:99154836-99155177 | Common:5; Rare:136; Clinvar (benign):3 | ||||
| chr2:99180962-99181273 | Common:2; Rare:91 | ||||
| chr2:99181291-99181521 | Rare:51 | ||||
| chr2:99336067-99336184 | Rare:33 | ||||
| chr2:99336250-99336651 | Common:2; Rare:116 | ||||
| chr2:99337200-99337850 | Common:1; Rare:211 | ||||
| chr2:99489326-99489510 | Common:3; Rare:60 | ||||
| chr2:99489523-99489746 | Common:2; Rare:72 | ||||
| chr2:99489937-99490409 | Common:2; Rare:182 | ||||
| chr2:99490496-99490639 | Rare:36 |