| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170554155-170554412 | Common:1; Rare:79 | ||||
| chr6:170584586-170584776 | Common:1; Rare:63 | ||||
| chr7:726616-726718 | Rare:39 | ||||
| chr7:1028307-1028523 | Common:1; Rare:75 | ||||
| chr7:1138198-1138521 | Common:2; Rare:93 | ||||
| chr7:1570020-1570087 | Common:1; Rare:24 | ||||
| chr7:1940485-1940688 | Rare:59 | ||||
| chr7:1980303-1980511 | Common:4; Rare:83 | ||||
| chr7:2242162-2242270 | Common:2; Rare:65 | ||||
| chr7:4775398-4775661 | Common:7; Rare:117; Clinvar:1 | ||||
| chr7:5513736-5514082 | Common:2; Rare:125 | ||||
| chr7:6009026-6009309 | Common:3; Rare:115; Clinvar:4; Clinvar (benign):14 | ||||
| chr7:6447897-6448096 | Common:2; Rare:81 | ||||
| chr7:6484111-6484282 | Common:1; Rare:78 | ||||
| chr7:6577356-6577509 | Common:1; Rare:54 |