| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134371518-134371601 | Common:2; Rare:44 | ||||
| chr5:134632754-134632918 | Rare:34 | ||||
| chr5:134648682-134648816 | Rare:39 | ||||
| chr5:134738432-134738573 | Rare:51 | ||||
| chr5:135399100-135399343 | Rare:64 | ||||
| chr5:138033058-138033142 | Common:1; Rare:31 | ||||
| chr5:138543110-138543522 | Common:2; Rare:128 | ||||
| chr5:138753277-138753503 | Common:2; Rare:77 | ||||
| chr5:139439453-139439606 | Common:1; Rare:43 | ||||
| chr5:139561733-139561800 | Rare:28 | ||||
| chr5:140303050-140303171 | Common:1; Rare:40 | ||||
| chr5:140557448-140557508 | Rare:29 | ||||
| chr5:140564317-140564449 | Common:1; Rare:41 | ||||
| chr5:140564594-140564837 | Rare:68 | ||||
| chr5:140647588-140647911 | Common:5; Rare:130; Clinvar:4; Clinvar (benign):3 |