| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:10457324-10457511 | Common:4; Rare:69 | ||||
| chr4:11428881-11429033 | Common:1; Rare:46 | ||||
| chr4:15681457-15681878 | Common:4; Rare:146 | ||||
| chr4:16083683-16084059 | Common:4; Rare:111 | ||||
| chr4:17614577-17614651 | Common:1; Rare:34 | ||||
| chr4:17810696-17811056 | Common:4; Rare:113 | ||||
| chr4:20700338-20700472 | Rare:59 | ||||
| chr4:25160405-25160704 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25377012-25377320 | Common:3; Rare:96 | ||||
| chr4:25914051-25914328 | Common:2; Rare:118 | ||||
| chr4:26320450-26320701 | Common:1; Rare:58 | ||||
| chr4:26583984-26584131 | Rare:29 | ||||
| chr4:37826481-37826729 | Common:7; Rare:83 | ||||
| chr4:38867565-38867826 | Common:2; Rare:88 | ||||
| chr4:39458843-39459120 | Common:3; Rare:157; Clinvar:1; Clinvar (benign):5 |