| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49120754-49121187 | Rare:120; Clinvar:1 | ||||
| chr3:49132613-49132903 | Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:49132979-49133173 | Rare:40; Clinvar:1 | ||||
| chr3:49166289-49166442 | Common:1; Rare:40 | ||||
| chr3:49199303-49199547 | Common:1; Rare:53 | ||||
| chr3:49340010-49340139 | Common:2; Rare:56 | ||||
| chr3:49358096-49358126 | Rare:15 | ||||
| chr3:49411882-49412427 | Common:2; Rare:200 | ||||
| chr3:49470019-49470325 | Common:1; Rare:89 | ||||
| chr3:49674225-49674402 | Common:1; Rare:70 | ||||
| chr3:49689482-49689605 | Rare:38 | ||||
| chr3:49723943-49724170 | Common:5; Rare:72 | ||||
| chr3:49856538-49856657 | Common:1; Rare:29 | ||||
| chr3:49939844-49940196 | Common:1; Rare:82 | ||||
| chr3:50267397-50267675 | Common:2; Rare:84 |