| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32391762-32391987 | Common:4; Rare:60 | ||||
| chr3:32502741-32502949 | Rare:60 | ||||
| chr3:32570287-32570365 | Common:1; Rare:40 | ||||
| chr3:32570636-32570953 | Common:1; Rare:144 | ||||
| chr3:33034676-33034831 | Common:1; Rare:31 | ||||
| chr3:33096759-33096974 | Common:1; Rare:54 | ||||
| chr3:33097087-33097234 | Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33218755-33218995 | Common:3; Rare:73 | ||||
| chr3:33277261-33277482 | Common:2; Rare:57 | ||||
| chr3:33289602-33289743 | Common:1; Rare:26 | ||||
| chr3:33372922-33373041 | Common:1; Rare:28 | ||||
| chr3:33440931-33441088 | Rare:31 | ||||
| chr3:33717987-33718303 | Rare:116 | ||||
| chr3:33798222-33798346 | Common:2; Rare:23 | ||||
| chr3:33798503-33798952 | Common:3; Rare:159 |