| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15681375-15681901 | Common:4; Rare:175 | ||||
| chr4:17614548-17614651 | Common:2; Rare:44 | ||||
| chr4:17810687-17811025 | Common:3; Rare:103 | ||||
| chr4:20700314-20700480 | Rare:70 | ||||
| chr4:24584453-24584871 | Common:1; Rare:107 | ||||
| chr4:25160405-25160704 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25914036-25914337 | Common:3; Rare:130 | ||||
| chr4:26320450-26320832 | Common:1; Rare:120 | ||||
| chr4:26320905-26321043 | Rare:49; Clinvar (benign):1 | ||||
| chr4:26860551-26860784 | Common:1; Rare:67 | ||||
| chr4:30719934-30720121 | Common:1; Rare:35 | ||||
| chr4:37826472-37826765 | Common:7; Rare:103 | ||||
| chr4:38867612-38867818 | Common:2; Rare:77 | ||||
| chr4:39366324-39366457 | Rare:43 | ||||
| chr4:39458849-39459122 | Common:3; Rare:155; Clinvar:1; Clinvar (benign):5 |