| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25312594-25312871 | Common:2; Rare:103 | ||||
| chr4:25377208-25377343 | Common:1; Rare:40 | ||||
| chr4:25913998-25914314 | Common:3; Rare:139 | ||||
| chr4:26319541-26319846 | Rare:84 | ||||
| chr4:26320447-26321090 | Common:1; Rare:224; Clinvar (benign):1 | ||||
| chr4:26583799-26584126 | Rare:65 | ||||
| chr4:26857516-26857764 | Common:4; Rare:75 | ||||
| chr4:26860568-26860841 | Common:3; Rare:95 | ||||
| chr4:26861452-26861646 | Common:1; Rare:51 | ||||
| chr4:30719821-30720221 | Common:3; Rare:104 | ||||
| chr4:30720264-30720428 | Rare:44 | ||||
| chr4:30721129-30721428 | Common:2; Rare:72 | ||||
| chr4:36243860-36244390 | Common:2; Rare:149 | ||||
| chr4:36244410-36244750 | Common:3; Rare:98 | ||||
| chr4:36332413-36332813 | Common:6; Rare:86 |