| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:5562685-5562908 | Rare:108 | ||||
| chr7:5781588-5781721 | Rare:63 | ||||
| chr7:6008988-6009400 | Common:8; Rare:332; Clinvar:32; Clinvar (benign):34; Clinvar (pathogenic):5 | ||||
| chr7:6059020-6059315 | Common:9; Rare:190 | ||||
| chr7:6104587-6105031 | Common:10; Rare:301 | ||||
| chr7:6272520-6272890 | Common:2; Rare:252 | ||||
| chr7:6374325-6374536 | Common:2; Rare:81 | ||||
| chr7:6447873-6448087 | Common:3; Rare:161 | ||||
| chr7:6482995-6483716 | Common:5; Rare:244 | ||||
| chr7:6483978-6484275 | Common:3; Rare:233 | ||||
| chr7:6577322-6577691 | Common:6; Rare:230 | ||||
| chr7:6589849-6590090 | Common:3; Rare:110 | ||||
| chr7:6590140-6590360 | Rare:135 | ||||
| chr7:6637249-6637370 | Rare:98 | ||||
| chr7:6637590-6638000 | Common:1; Rare:211 |