| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116525556-116525758 | Rare:37 | ||||
| chr7:116526202-116526683 | Common:3; Rare:131; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:116672167-116672514 | Common:1; Rare:79; Clinvar:2 | ||||
| chr7:116862432-116862639 | Common:2; Rare:73 | ||||
| chr7:118183964-118184199 | Common:2; Rare:89 | ||||
| chr7:120858076-120858090 | Rare:1 | ||||
| chr7:121396220-121396563 | Common:1; Rare:121 | ||||
| chr7:122144231-122144439 | Common:1; Rare:41 | ||||
| chr7:123748897-123749305 | Common:3; Rare:146 | ||||
| chr7:124929785-124929894 | Common:2; Rare:32 | ||||
| chr7:127585584-127585689 | Rare:33 | ||||
| chr7:127588283-127588443 | Rare:61 | ||||
| chr7:127651820-127652273 | Common:3; Rare:131 | ||||
| chr7:128455623-128455903 | Common:4; Rare:121 | ||||
| chr7:128476596-128476849 | Common:2; Rare:92 |