| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:124712633-124712850 | Common:1; Rare:65 | ||||
| chr4:127632808-127632966 | Common:1; Rare:38 | ||||
| chr4:127880764-127880930 | Rare:61 | ||||
| chr4:127965896-127965945 | Common:1; Rare:6; Clinvar (benign):1 | ||||
| chr4:128060994-128061380 | Common:1; Rare:132 | ||||
| chr4:128286674-128286722 | Rare:7 | ||||
| chr4:128287789-128288066 | Common:3; Rare:103 | ||||
| chr4:128288168-128288364 | Common:5; Rare:71 | ||||
| chr4:128809547-128809825 | Common:1; Rare:87 | ||||
| chr4:128811136-128811341 | Rare:46 | ||||
| chr4:129093411-129093741 | Common:2; Rare:93 | ||||
| chr4:129096067-129096175 | Common:1; Rare:24 | ||||
| chr4:133149111-133149295 | Common:2; Rare:53 | ||||
| chr4:137532379-137532656 | Common:1; Rare:43 | ||||
| chr4:139015439-139015799 | Common:2; Rare:118 |