| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:71582741-71583574 | Common:5; Rare:511 | ||||
| chr3:71583568-71583833 | Common:3; Rare:241 | ||||
| chr3:71583921-71584271 | Common:5; Rare:195; Clinvar:5; Clinvar (benign):3 | ||||
| chr3:71725314-71725547 | Common:2; Rare:110 | ||||
| chr3:71753579-71753914 | Common:8; Rare:222 | ||||
| chr3:71754100-71754820 | Common:1; Rare:332 | ||||
| chr3:72445987-72447040 | Common:13; Rare:654 | ||||
| chr3:72447110-72447367 | Rare:216 | ||||
| chr3:72848257-72848583 | Common:5; Rare:222 | ||||
| chr3:72996608-72997057 | Common:7; Rare:407 | ||||
| chr3:72997120-72997370 | Common:4; Rare:170 | ||||
| chr3:73624891-73624992 | Rare:38 | ||||
| chr3:73624917-73625115 | Common:4; Rare:51 | ||||
| chr3:73625190-73625720 | Common:1; Rare:117 | ||||
| chr3:75906380-75906830 | Common:2; Rare:108 |