| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83010745-83010911 | Rare:28 | ||||
| chr4:83455779-83456165 | Common:2; Rare:153 | ||||
| chr4:83485068-83485287 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:83535909-83536105 | Common:2; Rare:53 | ||||
| chr4:84966643-84966865 | Rare:55 | ||||
| chr4:86594055-86594378 | Rare:103 | ||||
| chr4:86849001-86849141 | Common:1; Rare:40 | ||||
| chr4:86849348-86849491 | Common:2; Rare:29 | ||||
| chr4:86934884-86935148 | Common:2; Rare:109 | ||||
| chr4:86936177-86936358 | Rare:39 | ||||
| chr4:87006876-87007190 | Common:4; Rare:79 | ||||
| chr4:87391111-87391346 | Common:2; Rare:78 | ||||
| chr4:87422516-87422728 | Common:1; Rare:59 | ||||
| chr4:87529050-87529598 | Common:5; Rare:94 | ||||
| chr4:88284534-88284912 | Common:2; Rare:89 |