| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77862632-77862900 | Common:3; Rare:104 | ||||
| chr4:78939379-78939533 | Common:1; Rare:73 | ||||
| chr4:80266432-80266827 | Common:3; Rare:103 | ||||
| chr4:82373905-82374160 | Common:2; Rare:78 | ||||
| chr4:82430447-82430836 | Common:3; Rare:136 | ||||
| chr4:82900469-82900823 | Rare:112 | ||||
| chr4:83455808-83456115 | Common:2; Rare:122 | ||||
| chr4:84966643-84966821 | Rare:44 | ||||
| chr4:86594041-86594358 | Rare:103 | ||||
| chr4:86934708-86935054 | Common:2; Rare:112 | ||||
| chr4:86936159-86936293 | Rare:35 | ||||
| chr4:88007455-88007690 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:88523691-88523848 | Common:2; Rare:55 | ||||
| chr4:88592307-88592542 | Common:1; Rare:73 | ||||
| chr4:89111393-89111577 | Common:2; Rare:69 |