| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:45111665-45111852 | Common:2; Rare:70 | ||||
| chr7:45921266-45921409 | Rare:37 | ||||
| chr7:47481256-47481437 | Rare:31 | ||||
| chr7:47582059-47582364 | Common:1; Rare:89 | ||||
| chr7:47582479-47582706 | Rare:53 | ||||
| chr7:47979500-47979726 | Rare:86 | ||||
| chr7:48089004-48089293 | Common:4; Rare:76 | ||||
| chr7:50450306-50450453 | Common:1; Rare:59 | ||||
| chr7:51316629-51316994 | Common:5; Rare:117 | ||||
| chr7:55018936-55019267 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:55365915-55366085 | Rare:73 | ||||
| chr7:55366258-55366375 | Common:1; Rare:42 | ||||
| chr7:55572312-55572587 | Common:1; Rare:106 | ||||
| chr7:55964406-55964603 | Rare:62 | ||||
| chr7:56051404-56051845 | Common:1; Rare:166; Clinvar:5; Clinvar (benign):1 |