| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17614547-17614651 | Common:2; Rare:44 | ||||
| chr4:24584462-24584734 | Common:1; Rare:83 | ||||
| chr4:25160384-25160727 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233835-25234105 | Rare:108 | ||||
| chr4:25312516-25312818 | Common:2; Rare:92 | ||||
| chr4:25779038-25779082 | Common:1; Rare:8 | ||||
| chr4:25861026-25861127 | Common:1; Rare:26 | ||||
| chr4:25862806-25863087 | Common:1; Rare:56 | ||||
| chr4:25913402-25913460 | Common:2; Rare:12 | ||||
| chr4:25914016-25914275 | Common:3; Rare:116 | ||||
| chr4:26320798-26321038 | Rare:94; Clinvar (benign):1 | ||||
| chr4:26857483-26857753 | Common:4; Rare:78 | ||||
| chr4:26860545-26860873 | Common:4; Rare:112 | ||||
| chr4:37826534-37826724 | Common:6; Rare:68 | ||||
| chr4:38804784-38805091 | Common:2; Rare:42 |