| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:18243886-18244056 | Common:1; Rare:24 | ||||
| chr2:18244827-18244895 | Rare:14 | ||||
| chr2:18244954-18245109 | Rare:30 | ||||
| chr2:18245568-18245587 | Rare:2 | ||||
| chr2:18262774-18262821 | Common:1; Rare:12 | ||||
| chr2:18299977-18300073 | Rare:25 | ||||
| chr2:18311511-18311657 | Rare:21 | ||||
| chr2:19347911-19348191 | Common:1; Rare:95 | ||||
| chr2:19363056-19363114 | Rare:10 | ||||
| chr2:19868772-19868898 | Rare:33 | ||||
| chr2:19902548-19902664 | Rare:23 | ||||
| chr2:19933283-19933460 | Common:1; Rare:52 | ||||
| chr2:19933482-19933970 | Common:3; Rare:89; Clinvar (benign):1 | ||||
| chr2:19971824-19972056 | Rare:39 | ||||
| chr2:19989455-19989509 | Rare:12 |