| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184174783-184174978 | Common:1; Rare:54 | ||||
| chr3:184248902-184249008 | Rare:53; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:184249512-184249689 | Rare:44 | ||||
| chr3:184314394-184314663 | Common:3; Rare:79 | ||||
| chr3:184325368-184325509 | Common:1; Rare:57 | ||||
| chr3:184711981-184712267 | Common:1; Rare:93 | ||||
| chr3:185282928-185283003 | Common:1; Rare:17 | ||||
| chr3:185824947-185825234 | Rare:86 | ||||
| chr3:186567322-186567446 | Common:1; Rare:26 | ||||
| chr3:186806432-186806607 | Rare:60 | ||||
| chr3:193593108-193593183 | Rare:20 | ||||
| chr3:195271071-195271304 | Common:1; Rare:94 | ||||
| chr3:196287581-196287812 | Common:1; Rare:69 | ||||
| chr3:196318144-196318335 | Common:1; Rare:86 | ||||
| chr3:196568527-196568652 | Common:2; Rare:31 |