| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131381459-131381794 | Common:3; Rare:82 | ||||
| chr3:131502765-131503013 | Common:1; Rare:101 | ||||
| chr3:132417161-132417534 | Common:5; Rare:122 | ||||
| chr3:132659799-132659890 | Common:3; Rare:18 | ||||
| chr3:133661852-133662021 | Rare:39 | ||||
| chr3:134485694-134485766 | Rare:29 | ||||
| chr3:134485956-134486260 | Common:3; Rare:107 | ||||
| chr3:136250295-136250372 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:136752340-136752671 | Common:1; Rare:109 | ||||
| chr3:136862000-136862275 | Common:1; Rare:85 | ||||
| chr3:136957711-136958032 | Common:1; Rare:62 | ||||
| chr3:138187156-138187372 | Common:1; Rare:57 | ||||
| chr3:138594209-138594442 | Rare:65 | ||||
| chr3:138608958-138609091 | Rare:40 | ||||
| chr3:138834874-138835066 | Rare:69 |