| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:132597135-132597275 | Common:1; Rare:17 | ||||
| chr3:132659799-132659914 | Common:3; Rare:24 | ||||
| chr3:132722127-132722225 | Common:1; Rare:42; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:133661849-133662010 | Rare:37 | ||||
| chr3:134485461-134485766 | Rare:74 | ||||
| chr3:134485964-134486456 | Common:6; Rare:160 | ||||
| chr3:136752295-136752671 | Common:1; Rare:122 | ||||
| chr3:136862016-136862281 | Common:1; Rare:80 | ||||
| chr3:138115548-138115713 | Common:4; Rare:44 | ||||
| chr3:138594209-138594442 | Rare:65 | ||||
| chr3:138834883-138835069 | Rare:65 | ||||
| chr3:139389568-139389875 | Common:2; Rare:98 | ||||
| chr3:141231688-141231894 | Common:1; Rare:72 | ||||
| chr3:141368260-141368572 | Rare:68 | ||||
| chr3:141486867-141487100 | Common:1; Rare:83 |