| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26319400-26319753 | Rare:98 | ||||
| chr4:26320619-26320745 | Common:1; Rare:46 | ||||
| chr4:26320748-26321043 | Rare:125; Clinvar (benign):1 | ||||
| chr4:26583892-26584131 | Rare:51 | ||||
| chr4:26857420-26857780 | Common:4; Rare:97 | ||||
| chr4:26860568-26860807 | Common:1; Rare:78 | ||||
| chr4:30719837-30720083 | Common:2; Rare:50 | ||||
| chr4:30720230-30720417 | Common:1; Rare:49 | ||||
| chr4:30721194-30721428 | Common:2; Rare:58 | ||||
| chr4:30721781-30722134 | Common:1; Rare:97 | ||||
| chr4:36243844-36244152 | Common:2; Rare:70 | ||||
| chr4:36244268-36244635 | Common:3; Rare:124 | ||||
| chr4:36244773-36244934 | Common:1; Rare:29 | ||||
| chr4:37826538-37826760 | Common:6; Rare:82 | ||||
| chr4:37890858-37891257 | Common:4; Rare:110 |