| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151736463-151736654 | Rare:32 | ||||
| chr7:152025569-152025879 | Common:1; Rare:112 | ||||
| chr7:152113083-152113261 | Rare:36 | ||||
| chr7:152676081-152676323 | Common:2; Rare:111; Clinvar (benign):12 | ||||
| chr7:152759597-152759859 | Common:4; Rare:97 | ||||
| chr7:155003330-155003537 | Common:7; Rare:85 | ||||
| chr7:155297638-155297884 | Common:3; Rare:88 | ||||
| chr7:155644349-155644502 | Common:1; Rare:38 | ||||
| chr7:155644613-155644882 | Common:4; Rare:90 | ||||
| chr7:156640520-156640708 | Common:4; Rare:103 | ||||
| chr7:156950207-156950425 | Common:2; Rare:94 | ||||
| chr7:157336761-157337017 | Common:1; Rare:112 | ||||
| chr7:158704764-158705114 | Common:1; Rare:118 | ||||
| chr7:158856420-158856747 | Common:7; Rare:115 | ||||
| chr8:232145-232403 | Common:3; Rare:102 |