| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:127880765-127880913 | Rare:54 | ||||
| chr4:128061248-128061348 | Rare:37 | ||||
| chr4:129093422-129093731 | Common:2; Rare:87 | ||||
| chr4:129096065-129096175 | Common:1; Rare:25 | ||||
| chr4:139301301-139301538 | Common:3; Rare:71 | ||||
| chr4:139453679-139453696 | Rare:7 | ||||
| chr4:139453697-139454204 | Common:4; Rare:137; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373384-140373713 | Common:3; Rare:134 | ||||
| chr4:140523977-140524198 | Common:2; Rare:64 | ||||
| chr4:142405400-142405543 | Rare:24 | ||||
| chr4:143337146-143337193 | Rare:21 | ||||
| chr4:144645882-144646184 | Common:1; Rare:81 | ||||
| chr4:145098143-145098350 | Rare:73 | ||||
| chr4:145482859-145483001 | Rare:21 | ||||
| chr4:145619340-145619396 | Rare:19 |