| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25160340-25160736 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233843-25234065 | Rare:94 | ||||
| chr4:25862694-25863011 | Rare:72 | ||||
| chr4:25914038-25914330 | Common:2; Rare:124 | ||||
| chr4:26320648-26321041 | Common:1; Rare:158; Clinvar (benign):1 | ||||
| chr4:26857489-26857768 | Common:4; Rare:82 | ||||
| chr4:26860568-26860859 | Common:3; Rare:100 | ||||
| chr4:37826615-37826729 | Common:1; Rare:41 | ||||
| chr4:38856800-38856952 | Common:5; Rare:25 | ||||
| chr4:39044518-39044849 | Common:6; Rare:102 | ||||
| chr4:39182320-39182554 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39458810-39459156 | Common:3; Rare:185; Clinvar:4; Clinvar (benign):6 | ||||
| chr4:39527269-39527328 | Common:2; Rare:14 | ||||
| chr4:39527342-39527780 | Common:4; Rare:118 | ||||
| chr4:39527918-39528047 | Rare:31 |