| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:149126258-149126429 | Common:6; Rare:52 | ||||
| chr7:149147284-149147466 | Common:3; Rare:43 | ||||
| chr7:149873694-149874047 | Common:4; Rare:125 | ||||
| chr7:151057884-151058200 | Common:3; Rare:81 | ||||
| chr7:152025549-152025697 | Common:1; Rare:57 | ||||
| chr7:155003388-155003477 | Common:3; Rare:51 | ||||
| chr7:155644399-155644460 | Rare:9 | ||||
| chr7:155644617-155644854 | Common:4; Rare:79 | ||||
| chr7:156640560-156640784 | Common:2; Rare:108 | ||||
| chr7:157336907-157337016 | Rare:36 | ||||
| chr8:1755637-1755776 | Common:2; Rare:42 | ||||
| chr8:6406529-6406668 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708171-6708412 | Common:3; Rare:108 | ||||
| chr8:9151631-9151744 | Common:1; Rare:35 | ||||
| chr8:10839806-10839963 | Rare:66 |