| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82373947-82374309 | Common:3; Rare:104 | ||||
| chr4:82430436-82430860 | Common:3; Rare:150 | ||||
| chr4:82891093-82891419 | Common:2; Rare:130 | ||||
| chr4:82900473-82900741 | Rare:76 | ||||
| chr4:83012905-83013089 | Common:1; Rare:49 | ||||
| chr4:83034873-83035222 | Common:1; Rare:86 | ||||
| chr4:83455785-83456160 | Common:2; Rare:147 | ||||
| chr4:85778132-85778748 | Common:1; Rare:84 | ||||
| chr4:86936160-86936353 | Rare:43 | ||||
| chr4:87007150-87007254 | Rare:33 | ||||
| chr4:88523600-88523875 | Common:2; Rare:90 | ||||
| chr4:88592283-88592542 | Common:1; Rare:80 | ||||
| chr4:88697750-88697919 | Common:2; Rare:60 | ||||
| chr4:89111418-89111594 | Common:1; Rare:66 | ||||
| chr4:89836908-89837274 | Common:3; Rare:119; Clinvar:5; Clinvar (benign):1 |