| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:131502793-131502995 | Common:1; Rare:91 | ||||
| chr3:132659799-132659907 | Common:3; Rare:22 | ||||
| chr3:132722108-132722220 | Common:1; Rare:50; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:133661813-133662010 | Rare:47 | ||||
| chr3:134374369-134374667 | Common:2; Rare:86 | ||||
| chr3:134485694-134485766 | Rare:29 | ||||
| chr3:134485945-134486229 | Common:3; Rare:98 | ||||
| chr3:134650975-134651097 | Common:1; Rare:52 | ||||
| chr3:134795136-134795566 | Common:2; Rare:94 | ||||
| chr3:136196556-136196740 | Rare:56 | ||||
| chr3:136752281-136752736 | Common:1; Rare:149 | ||||
| chr3:136861995-136862298 | Common:1; Rare:99 | ||||
| chr3:136957717-136958056 | Common:1; Rare:61 | ||||
| chr3:138115383-138115424 | Rare:11 | ||||
| chr3:138115585-138115690 | Common:4; Rare:26 |