| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22822676-22822969 | Common:3; Rare:112 | ||||
| chr7:23014026-23014329 | Common:2; Rare:119; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105616-23106460 | Common:6; Rare:282; Clinvar:5; Clinvar (benign):3 | ||||
| chr7:23181752-23182257 | Common:5; Rare:199 | ||||
| chr7:23299197-23299266 | Rare:21 | ||||
| chr7:23299275-23299378 | Common:1; Rare:68 | ||||
| chr7:23531897-23532119 | Common:2; Rare:89 | ||||
| chr7:23597204-23597771 | Common:2; Rare:175 | ||||
| chr7:23598089-23598170 | Rare:21 | ||||
| chr7:23680001-23680268 | Common:6; Rare:87 | ||||
| chr7:23710054-23710363 | Common:7; Rare:145 | ||||
| chr7:24573183-24573341 | Common:1; Rare:68 | ||||
| chr7:24757395-24757517 | Common:2; Rare:37 | ||||
| chr7:24980108-24980360 | Common:6; Rare:104 | ||||
| chr7:25125200-25125450 | Rare:110; Clinvar:3 |