| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:127965920-127965993 | Rare:13 | ||||
| chr4:128287369-128287431 | Rare:16 | ||||
| chr4:128287438-128287667 | Common:1; Rare:82 | ||||
| chr4:128287767-128288008 | Common:3; Rare:95 | ||||
| chr4:128809469-128809851 | Common:1; Rare:117 | ||||
| chr4:128811070-128811324 | Rare:51 | ||||
| chr4:129093454-129093753 | Common:1; Rare:87 | ||||
| chr4:133149104-133149316 | Common:2; Rare:61 | ||||
| chr4:137531806-137532134 | Rare:101 | ||||
| chr4:137532368-137532734 | Common:3; Rare:65 | ||||
| chr4:138242248-138242599 | Common:1; Rare:75 | ||||
| chr4:139084168-139084447 | Common:2; Rare:114 | ||||
| chr4:139301214-139301612 | Common:5; Rare:115 | ||||
| chr4:139302451-139302573 | Common:1; Rare:26 | ||||
| chr4:139453724-139454237 | Common:3; Rare:145; Clinvar:10; Clinvar (benign):4 |