| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216694443-216694506 | Rare:11 | ||||
| chr2:216694519-216694569 | Rare:13 | ||||
| chr2:216694572-216694616 | Rare:9 | ||||
| chr2:216694629-216694773 | Rare:42 | ||||
| chr2:216694781-216695008 | Rare:41 | ||||
| chr2:216859887-216860236 | Common:1; Rare:113 | ||||
| chr2:217434190-217434362 | Rare:36 | ||||
| chr2:217756520-217756597 | Common:1; Rare:13 | ||||
| chr2:217903788-217903906 | Common:1; Rare:17 | ||||
| chr2:217920005-217920193 | Common:5; Rare:49 | ||||
| chr2:217978769-217978918 | Common:1; Rare:44 | ||||
| chr2:218217044-218217262 | Common:1; Rare:73 | ||||
| chr2:218270028-218270557 | Common:5; Rare:171; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:218280024-218280275 | Rare:70 | ||||
| chr2:218292477-218292593 | Rare:29 |