| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32502770-32503034 | Rare:62 | ||||
| chr3:32570636-32570958 | Common:1; Rare:144 | ||||
| chr3:32685050-32685394 | Rare:103 | ||||
| chr3:32818133-32818286 | Rare:75 | ||||
| chr3:33097088-33097272 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277270-33277509 | Common:3; Rare:69 | ||||
| chr3:33440856-33441076 | Common:2; Rare:45 | ||||
| chr3:33645207-33645567 | Common:1; Rare:60 | ||||
| chr3:33658997-33659237 | Common:3; Rare:49 | ||||
| chr3:33659505-33659783 | Common:1; Rare:64 | ||||
| chr3:33718050-33718309 | Rare:98 | ||||
| chr3:33798497-33798692 | Common:2; Rare:72 | ||||
| chr3:35639317-35639759 | Common:4; Rare:101 | ||||
| chr3:35639762-35639848 | Rare:18 | ||||
| chr3:35639850-35640033 | Common:2; Rare:40 |