| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140270116-140270352 | Rare:38 | ||||
| chr5:140589594-140589689 | Common:1; Rare:15 | ||||
| chr5:140657414-140657604 | Common:1; Rare:40 | ||||
| chr5:141528809-141529124 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:141656194-141656387 | Common:1; Rare:48; Clinvar:1 | ||||
| chr5:141955295-141955341 | Rare:15; Clinvar (pathogenic):1 | ||||
| chr5:141956190-141956332 | Rare:48 | ||||
| chr5:141957438-141957565 | Common:1; Rare:35 | ||||
| chr5:142132053-142132262 | Common:1; Rare:40 | ||||
| chr5:142798514-142798825 | Rare:54 | ||||
| chr5:148826379-148826633 | Common:3; Rare:63 | ||||
| chr5:148827676-148827837 | Rare:41 | ||||
| chr5:148834872-148834975 | Common:1; Rare:22 | ||||
| chr5:149428961-149429000 | Rare:7 | ||||
| chr5:149430513-149430721 | Rare:57 |