| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174284262-174284269 | Rare:1 | ||||
| chr4:177442377-177442554 | Rare:104; Clinvar:2 | ||||
| chr4:182143854-182143968 | Common:1; Rare:28 | ||||
| chr4:182144429-182144734 | Common:3; Rare:98 | ||||
| chr4:183659105-183659354 | Common:1; Rare:85 | ||||
| chr4:184474535-184474734 | Rare:52 | ||||
| chr4:184649430-184649796 | Common:4; Rare:116 | ||||
| chr4:184734125-184734430 | Common:6; Rare:91 | ||||
| chr4:185143136-185143270 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr4:185425877-185426252 | Common:3; Rare:110 | ||||
| chr4:186723743-186723937 | Common:5; Rare:81 | ||||
| chr4:189940639-189940955 | Common:9; Rare:114 | ||||
| chr5:218134-218352 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:443080-443272 | Common:10; Rare:87 | ||||
| chr5:892732-892949 | Common:2; Rare:83 |