| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:32487951-32488269 | Common:1; Rare:68 | ||||
| chr3:32570636-32570966 | Common:1; Rare:145 | ||||
| chr3:33097082-33097265 | Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:33277342-33277482 | Common:1; Rare:35 | ||||
| chr3:33439904-33440193 | Common:1; Rare:93 | ||||
| chr3:33798484-33798701 | Common:2; Rare:78 | ||||
| chr3:33799006-33799080 | Rare:28 | ||||
| chr3:36380476-36380550 | Common:1; Rare:22 | ||||
| chr3:36993064-36993580 | Common:2; Rare:179; Clinvar:32; Clinvar (benign):15; Clinvar (pathogenic):3 | ||||
| chr3:37176233-37176393 | Rare:52 | ||||
| chr3:37243166-37243603 | Common:1; Rare:123 | ||||
| chr3:38024501-38024667 | Common:1; Rare:64 | ||||
| chr3:38029612-38029864 | Common:1; Rare:51 | ||||
| chr3:39051939-39052068 | Common:1; Rare:48 | ||||
| chr3:39107562-39107684 | Common:2; Rare:39 |