| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:124712613-124712850 | Common:1; Rare:69 | ||||
| chr4:127880764-127880948 | Rare:65 | ||||
| chr4:127965896-127965990 | Common:1; Rare:15; Clinvar (benign):1 | ||||
| chr4:128060904-128061384 | Common:1; Rare:164 | ||||
| chr4:128287789-128288016 | Common:3; Rare:88 | ||||
| chr4:128288196-128288309 | Common:4; Rare:42 | ||||
| chr4:128811162-128811344 | Rare:40 | ||||
| chr4:129093436-129093741 | Common:2; Rare:87 | ||||
| chr4:129096119-129096164 | Common:1; Rare:13 | ||||
| chr4:137532378-137532755 | Common:2; Rare:65 | ||||
| chr4:139177216-139177456 | Rare:70 | ||||
| chr4:139301120-139301762 | Common:7; Rare:182 | ||||
| chr4:139302463-139302477 | Rare:4 | ||||
| chr4:139302480-139302564 | Common:1; Rare:11 | ||||
| chr4:139453665-139454210 | Common:5; Rare:157; Clinvar:10; Clinvar (benign):4 |