| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6009005-6009480 | Common:4; Rare:226; Clinvar:16; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr7:6009484-6009543 | Common:1; Rare:31 | ||||
| chr7:6059033-6059306 | Common:5; Rare:105 | ||||
| chr7:6104626-6105009 | Common:5; Rare:136 | ||||
| chr7:6272567-6272743 | Rare:84 | ||||
| chr7:6348951-6349236 | Common:3; Rare:103 | ||||
| chr7:6483970-6484263 | Common:2; Rare:131 | ||||
| chr7:6706929-6707099 | Rare:67 | ||||
| chr7:6826171-6826306 | Common:4; Rare:30 | ||||
| chr7:7182353-7182768 | Common:3; Rare:146 | ||||
| chr7:7566812-7567060 | Common:4; Rare:97 | ||||
| chr7:7968580-7968595 | Rare:5 | ||||
| chr7:8262126-8262310 | Rare:83 | ||||
| chr7:8262531-8262626 | Common:1; Rare:29 | ||||
| chr7:10940017-10940230 | Common:1; Rare:98; Clinvar (benign):3 |