| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33277313-33277476 | Common:1; Rare:41 | ||||
| chr3:33440351-33440476 | Rare:39 | ||||
| chr3:33717866-33718254 | Common:1; Rare:127 | ||||
| chr3:33798435-33798751 | Common:2; Rare:103 | ||||
| chr3:33798997-33799163 | Rare:52 | ||||
| chr3:36993067-36993580 | Common:2; Rare:179; Clinvar:32; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr3:37175509-37175612 | Common:1; Rare:22 | ||||
| chr3:37176124-37176367 | Common:1; Rare:67 | ||||
| chr3:37242941-37243578 | Common:5; Rare:176 | ||||
| chr3:37861719-37861895 | Common:1; Rare:40 | ||||
| chr3:37993955-37994171 | Common:1; Rare:56 | ||||
| chr3:38008139-38008210 | Rare:24 | ||||
| chr3:38010473-38010677 | Common:1; Rare:65 | ||||
| chr3:38024494-38024664 | Common:1; Rare:63 | ||||
| chr3:38029605-38029754 | Common:1; Rare:29 |