| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49021503-49021746 | Rare:57; Clinvar:1 | ||||
| chr3:49022011-49022176 | Rare:57; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49029324-49029573 | Common:2; Rare:172 | ||||
| chr3:49104726-49104976 | Rare:96; Clinvar (benign):3 | ||||
| chr3:49340026-49340127 | Common:2; Rare:43 | ||||
| chr3:49411906-49412435 | Common:2; Rare:198 | ||||
| chr3:49689459-49689565 | Rare:25 | ||||
| chr3:50299259-50299666 | Common:2; Rare:96 | ||||
| chr3:50350711-50350897 | Common:1; Rare:29 | ||||
| chr3:50569386-50569569 | Common:1; Rare:41 | ||||
| chr3:50611765-50611886 | Rare:28 | ||||
| chr3:51385015-51385324 | Rare:84 | ||||
| chr3:51983433-51983543 | Rare:24 | ||||
| chr3:51995857-51996032 | Common:2; Rare:65 | ||||
| chr3:52239038-52239264 | Common:2; Rare:77 |