| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134483204-134483395 | Rare:38 | ||||
| chr3:134485407-134485878 | Common:1; Rare:120 | ||||
| chr3:134485957-134486260 | Common:3; Rare:107 | ||||
| chr3:135965544-135965794 | Common:1; Rare:109 | ||||
| chr3:136196571-136196727 | Rare:46 | ||||
| chr3:136250260-136250426 | Common:2; Rare:72; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr3:136752229-136752671 | Common:1; Rare:142 | ||||
| chr3:136818969-136819197 | Common:4; Rare:112 | ||||
| chr3:136862001-136862298 | Common:1; Rare:96 | ||||
| chr3:138115594-138115716 | Common:3; Rare:29 | ||||
| chr3:138174844-138174996 | Common:1; Rare:33 | ||||
| chr3:138594209-138594445 | Rare:66 | ||||
| chr3:138834874-138835069 | Rare:71 | ||||
| chr3:139344437-139344617 | Rare:32 | ||||
| chr3:139389562-139389890 | Common:2; Rare:106 |