| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134004651-134004851 | Common:1; Rare:74 | ||||
| chr5:134648500-134648816 | Common:1; Rare:74 | ||||
| chr5:134845853-134846057 | Rare:92 | ||||
| chr5:138178953-138179178 | Common:2; Rare:47 | ||||
| chr5:138338260-138338283 | Common:1; Rare:11 | ||||
| chr5:138543183-138543481 | Common:2; Rare:95 | ||||
| chr5:139198289-139198525 | Rare:79; Clinvar (benign):1 | ||||
| chr5:140303069-140303233 | Common:1; Rare:48 | ||||
| chr5:140557437-140557506 | Rare:36 | ||||
| chr5:140647594-140647889 | Common:5; Rare:118; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691353-140691464 | Common:1; Rare:26; Clinvar:3 | ||||
| chr5:141636824-141636957 | Common:1; Rare:55 | ||||
| chr5:141923613-141923868 | Common:1; Rare:67 | ||||
| chr5:143404455-143404604 | Common:2; Rare:31 | ||||
| chr5:149345422-149345524 | Common:1; Rare:35 |