| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48918768-48918902 | Common:2; Rare:78 | ||||
| chr3:48989734-48989907 | Rare:48 | ||||
| chr3:49007032-49007411 | Common:2; Rare:130 | ||||
| chr3:49021503-49021768 | Rare:60; Clinvar:1 | ||||
| chr3:49022011-49022179 | Rare:59; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49104663-49104925 | Common:1; Rare:109; Clinvar:2; Clinvar (benign):6 | ||||
| chr3:49340026-49340124 | Common:2; Rare:43 | ||||
| chr3:49411902-49412449 | Common:2; Rare:202 | ||||
| chr3:49689459-49689593 | Rare:39 | ||||
| chr3:50299263-50299662 | Common:1; Rare:94 | ||||
| chr3:50340812-50340955 | Rare:45 | ||||
| chr3:50350705-50350908 | Common:1; Rare:31 | ||||
| chr3:50567674-50567868 | Rare:63 | ||||
| chr3:50569386-50569584 | Common:1; Rare:44 | ||||
| chr3:50611765-50611886 | Rare:28 |