| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:52051289-52051504 | Common:1; Rare:50 | ||||
| chr4:52659234-52659439 | Common:1; Rare:68 | ||||
| chr4:53591570-53591640 | Rare:17 | ||||
| chr4:54064212-54064682 | Common:3; Rare:137 | ||||
| chr4:55546814-55546992 | Common:2; Rare:61 | ||||
| chr4:55948714-55948928 | Common:1; Rare:42 | ||||
| chr4:56387409-56387522 | Rare:39 | ||||
| chr4:56435473-56435973 | Common:6; Rare:164 | ||||
| chr4:56436045-56436315 | Rare:101 | ||||
| chr4:56467518-56467699 | Common:2; Rare:75; Clinvar (benign):5 | ||||
| chr4:56530355-56530636 | Common:6; Rare:65 | ||||
| chr4:56656301-56656548 | Common:3; Rare:41 | ||||
| chr4:56656551-56656626 | Rare:15 | ||||
| chr4:56681194-56681534 | Common:1; Rare:53 | ||||
| chr4:56977006-56977308 | Common:3; Rare:130 |