| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37826538-37826729 | Common:6; Rare:68 | ||||
| chr4:38664217-38664346 | Common:1; Rare:40 | ||||
| chr4:38867583-38867818 | Common:2; Rare:83 | ||||
| chr4:39062320-39062578 | Common:2; Rare:60 | ||||
| chr4:39182199-39182548 | Rare:77; Clinvar:2 | ||||
| chr4:39366299-39366419 | Common:1; Rare:34 | ||||
| chr4:39458393-39459128 | Common:7; Rare:290; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527383-39527801 | Common:2; Rare:116 | ||||
| chr4:39527925-39528013 | Rare:21 | ||||
| chr4:39638783-39639206 | Common:1; Rare:158 | ||||
| chr4:39697931-39698334 | Common:2; Rare:155 | ||||
| chr4:40056591-40057014 | Common:4; Rare:124 | ||||
| chr4:41214420-41214716 | Common:5; Rare:78 | ||||
| chr4:41216681-41216812 | Common:2; Rare:21 | ||||
| chr4:41256714-41257025 | Common:3; Rare:99; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |