| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:1871845-1872245 | Common:3; Rare:154 | ||||
| chr4:2008929-2009038 | Rare:46 | ||||
| chr4:2009230-2009360 | Common:1; Rare:39 | ||||
| chr4:2009558-2009687 | Rare:33 | ||||
| chr4:2041729-2042061 | Common:1; Rare:103 | ||||
| chr4:2242047-2242435 | Common:1; Rare:139 | ||||
| chr4:2262058-2262273 | Rare:83 | ||||
| chr4:2262292-2262598 | Common:4; Rare:116 | ||||
| chr4:2462383-2462648 | Common:1; Rare:89 | ||||
| chr4:2468840-2469181 | Common:4; Rare:134 | ||||
| chr4:2469595-2470032 | Common:2; Rare:203 | ||||
| chr4:2755910-2756210 | Common:3; Rare:96 | ||||
| chr4:2756313-2756583 | Common:3; Rare:53 | ||||
| chr4:2817970-2818250 | Common:1; Rare:72 | ||||
| chr4:2818513-2818913 | Common:7; Rare:107; Clinvar (benign):2 |