| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:26201423-26201821 | Common:2; Rare:190 | ||||
| chr7:27113832-27113951 | Rare:28 | ||||
| chr7:27185202-27185391 | Common:1; Rare:77 | ||||
| chr7:30504594-30504662 | Rare:25 | ||||
| chr7:30594738-30595107 | Common:6; Rare:173; Clinvar:9; Clinvar (benign):14 | ||||
| chr7:40134582-40134766 | Rare:58 | ||||
| chr7:42932160-42932413 | Rare:103 | ||||
| chr7:43926381-43926452 | Rare:23 | ||||
| chr7:44573844-44574053 | Common:3; Rare:71 | ||||
| chr7:56051384-56051857 | Common:1; Rare:179; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:73683437-73683622 | Common:3; Rare:75 | ||||
| chr7:74254335-74254535 | Rare:93 | ||||
| chr7:76047770-76048183 | Common:2; Rare:123 | ||||
| chr7:77696253-77696467 | Rare:87 | ||||
| chr7:79453778-79454047 | Common:2; Rare:68 |