| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138875197-138875613 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr5:138875618-138875688 | Rare:10 | ||||
| chr5:139198284-139198556 | Rare:93; Clinvar (benign):1 | ||||
| chr5:139273980-139274142 | Rare:74 | ||||
| chr5:139341681-139341980 | Common:1; Rare:80 | ||||
| chr5:139404069-139404288 | Rare:60 | ||||
| chr5:139439441-139439615 | Common:2; Rare:47 | ||||
| chr5:139561094-139561397 | Common:1; Rare:121 | ||||
| chr5:139561733-139561803 | Rare:28 | ||||
| chr5:140303065-140303177 | Common:1; Rare:32 | ||||
| chr5:140346597-140346686 | Rare:25 | ||||
| chr5:140401410-140401836 | Common:3; Rare:87 | ||||
| chr5:140557427-140557530 | Common:1; Rare:60 | ||||
| chr5:140564365-140564509 | Common:1; Rare:38 | ||||
| chr5:140564556-140564837 | Rare:74 |