| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33114513-33114548 | Common:1; Rare:12; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:33277325-33277495 | Common:1; Rare:46 | ||||
| chr3:33645436-33645541 | Rare:13 | ||||
| chr3:33717939-33718286 | Rare:122 | ||||
| chr3:33798287-33798870 | Common:4; Rare:173 | ||||
| chr3:33798985-33799054 | Rare:25 | ||||
| chr3:36992567-36992676 | Rare:36 | ||||
| chr3:36993051-36993620 | Common:2; Rare:205; Clinvar:39; Clinvar (benign):20; Clinvar (pathogenic):4 | ||||
| chr3:37065881-37066192 | Common:2; Rare:71 | ||||
| chr3:37176124-37176393 | Common:1; Rare:74 | ||||
| chr3:37243143-37243603 | Common:1; Rare:134 | ||||
| chr3:37861706-37861905 | Common:1; Rare:42 | ||||
| chr3:37990622-37990827 | Common:1; Rare:47 | ||||
| chr3:37991125-37991582 | Common:2; Rare:85 | ||||
| chr3:37992692-37992949 | Rare:32 |