| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:30676654-30676723 | Rare:13 | ||||
| chr3:30678578-30678703 | Common:1; Rare:23 | ||||
| chr3:30680379-30680670 | Common:1; Rare:44 | ||||
| chr3:30681354-30681638 | Common:2; Rare:45 | ||||
| chr3:30681722-30681793 | Common:1; Rare:14 | ||||
| chr3:30681918-30682182 | Common:1; Rare:62 | ||||
| chr3:30684804-30685061 | Common:1; Rare:38 | ||||
| chr3:30688959-30689041 | Rare:18 | ||||
| chr3:30689381-30689640 | Common:1; Rare:53 | ||||
| chr3:30705499-30705760 | Common:1; Rare:48 | ||||
| chr3:31004479-31004655 | Rare:27 | ||||
| chr3:31093117-31093380 | Common:1; Rare:34 | ||||
| chr3:31531711-31531979 | Common:3; Rare:62 | ||||
| chr3:31579514-31580112 | Common:5; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:31620744-31620900 | Common:1; Rare:35 |