| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151028127-151028464 | Rare:107 | ||||
| chr7:151057856-151058205 | Common:3; Rare:99 | ||||
| chr7:151080788-151080972 | Rare:58 | ||||
| chr7:151232396-151232525 | Rare:41 | ||||
| chr7:152435947-152436275 | Rare:115 | ||||
| chr7:155644170-155644229 | Rare:16 | ||||
| chr7:155644357-155644724 | Common:2; Rare:129 | ||||
| chr7:157336778-157337090 | Common:3; Rare:150; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158704800-158705131 | Common:1; Rare:108 | ||||
| chr7:158856425-158856695 | Common:7; Rare:97 | ||||
| chr8:232226-232462 | Common:2; Rare:100 | ||||
| chr8:406717-406999 | Common:4; Rare:135 | ||||
| chr8:6406523-6406670 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:10839829-10840116 | Common:3; Rare:91 | ||||
| chr8:11704107-11704236 | Common:1; Rare:32 |