| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49674183-49674456 | Common:1; Rare:106 | ||||
| chr3:49674608-49674643 | Rare:15 | ||||
| chr3:49689447-49689694 | Common:1; Rare:68 | ||||
| chr3:49719607-49719817 | Common:1; Rare:60 | ||||
| chr3:49723382-49723616 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:49723901-49724321 | Common:10; Rare:143 | ||||
| chr3:49786467-49786846 | Common:2; Rare:124 | ||||
| chr3:49802681-49802870 | Common:1; Rare:32 | ||||
| chr3:49803088-49803335 | Common:3; Rare:84 | ||||
| chr3:49803660-49804013 | Common:2; Rare:63 | ||||
| chr3:49806325-49806540 | Rare:50 | ||||
| chr3:49813828-49814079 | Common:1; Rare:35 | ||||
| chr3:49856441-49856782 | Common:2; Rare:112 | ||||
| chr3:49903849-49904099 | Common:1; Rare:72 | ||||
| chr3:49929187-49929452 | Common:1; Rare:58 |