| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134485986-134486229 | Common:2; Rare:77 | ||||
| chr3:136250255-136250373 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:136752368-136752666 | Common:1; Rare:103 | ||||
| chr3:136862027-136862276 | Common:1; Rare:70 | ||||
| chr3:138174892-138174956 | Common:1; Rare:13 | ||||
| chr3:138187227-138187557 | Rare:96 | ||||
| chr3:138594209-138594445 | Rare:66 | ||||
| chr3:138608618-138608849 | Rare:44 | ||||
| chr3:138608937-138609127 | Common:1; Rare:53 | ||||
| chr3:139389617-139389853 | Common:1; Rare:74 | ||||
| chr3:140941641-140941926 | Common:2; Rare:106 | ||||
| chr3:141231652-141231840 | Common:2; Rare:61 | ||||
| chr3:141402235-141402402 | Common:2; Rare:49 | ||||
| chr3:141486879-141487078 | Common:1; Rare:63 | ||||
| chr3:141738093-141738353 | Common:2; Rare:111 |