| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15655289-15655477 | Common:1; Rare:84 | ||||
| chr4:15681560-15681866 | Common:3; Rare:107 | ||||
| chr4:15703011-15703125 | Common:1; Rare:24 | ||||
| chr4:17614548-17614647 | Common:2; Rare:43 | ||||
| chr4:17810676-17811072 | Common:4; Rare:126 | ||||
| chr4:20700245-20700495 | Common:1; Rare:112 | ||||
| chr4:24584447-24584725 | Common:1; Rare:85 | ||||
| chr4:25160411-25160725 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:26320755-26321057 | Rare:127; Clinvar (benign):1 | ||||
| chr4:30720251-30720422 | Common:1; Rare:46 | ||||
| chr4:37826534-37826729 | Common:6; Rare:70 | ||||
| chr4:38867576-38867822 | Common:2; Rare:86 | ||||
| chr4:39182340-39182548 | Rare:46; Clinvar:2 | ||||
| chr4:39458864-39459112 | Common:3; Rare:140; Clinvar (benign):5 | ||||
| chr4:39527383-39527763 | Common:2; Rare:96 |