| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77862641-77862861 | Common:3; Rare:75 | ||||
| chr4:81471790-81472075 | Common:1; Rare:89 | ||||
| chr4:82373941-82374186 | Common:2; Rare:71 | ||||
| chr4:82429367-82429634 | Common:1; Rare:164; Clinvar:13; Clinvar (benign):5 | ||||
| chr4:82891037-82891317 | Common:1; Rare:108 | ||||
| chr4:82900457-82900732 | Rare:79 | ||||
| chr4:82900909-82901062 | Rare:61 | ||||
| chr4:83034873-83035221 | Common:1; Rare:85 | ||||
| chr4:83455787-83456078 | Common:2; Rare:110 | ||||
| chr4:84966651-84966732 | Rare:20 | ||||
| chr4:85474970-85475255 | Common:2; Rare:48 | ||||
| chr4:86594055-86594364 | Rare:99 | ||||
| chr4:86936177-86936331 | Rare:35 | ||||
| chr4:87006880-87007040 | Common:2; Rare:38 | ||||
| chr4:87391111-87391288 | Common:1; Rare:57 |