| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122152280-122152416 | Common:2; Rare:57 | ||||
| chr4:122379366-122379581 | Rare:79 | ||||
| chr4:122732445-122732768 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922966-122923120 | Common:2; Rare:45 | ||||
| chr4:123399348-123399653 | Common:1; Rare:92 | ||||
| chr4:127880821-127880934 | Rare:35 | ||||
| chr4:128060978-128061325 | Common:1; Rare:126 | ||||
| chr4:128287789-128287907 | Common:1; Rare:57 | ||||
| chr4:128811174-128811313 | Rare:28 | ||||
| chr4:129093494-129093712 | Rare:69 | ||||
| chr4:129096113-129096184 | Common:1; Rare:22 | ||||
| chr4:133149111-133149301 | Common:2; Rare:57 | ||||
| chr4:139084192-139084270 | Rare:37 | ||||
| chr4:139177192-139177456 | Rare:78 | ||||
| chr4:139301291-139301531 | Common:4; Rare:73 |