| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134374423-134374705 | Common:2; Rare:87 | ||||
| chr3:134485335-134485772 | Rare:101 | ||||
| chr3:134485957-134486307 | Common:3; Rare:121 | ||||
| chr3:134794993-134795177 | Rare:40 | ||||
| chr3:134795183-134795402 | Common:1; Rare:46 | ||||
| chr3:135965522-135965844 | Common:1; Rare:126 | ||||
| chr3:136196282-136196425 | Rare:59 | ||||
| chr3:136196531-136196701 | Rare:60 | ||||
| chr3:136250234-136250392 | Common:3; Rare:67; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr3:136752217-136752768 | Common:2; Rare:180 | ||||
| chr3:136861984-136862312 | Common:1; Rare:105 | ||||
| chr3:138174638-138174960 | Common:4; Rare:107 | ||||
| chr3:138329749-138330025 | Common:1; Rare:63 | ||||
| chr3:138348378-138348747 | Common:2; Rare:98 | ||||
| chr3:138594202-138594502 | Rare:98 |