| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82429247-82429656 | Common:2; Rare:218; Clinvar:13; Clinvar (benign):8 | ||||
| chr4:82429957-82430375 | Common:1; Rare:123 | ||||
| chr4:82430376-82430910 | Common:3; Rare:184 | ||||
| chr4:82900403-82900790 | Common:1; Rare:118 | ||||
| chr4:82900900-82901035 | Rare:57 | ||||
| chr4:83114723-83114771 | Common:2; Rare:11 | ||||
| chr4:83455796-83456078 | Common:2; Rare:109 | ||||
| chr4:84966641-84966799 | Rare:39 | ||||
| chr4:85474959-85475274 | Common:3; Rare:56 | ||||
| chr4:86594041-86594351 | Rare:98 | ||||
| chr4:86934736-86935061 | Common:2; Rare:111 | ||||
| chr4:86936202-86936434 | Common:1; Rare:44 | ||||
| chr4:87007143-87007324 | Common:1; Rare:65 | ||||
| chr4:87422549-87422726 | Common:1; Rare:47 | ||||
| chr4:88007516-88007692 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):1 |