| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122732429-122732768 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922902-122923128 | Common:2; Rare:61 | ||||
| chr4:123399348-123399653 | Common:1; Rare:92 | ||||
| chr4:128287789-128288058 | Common:3; Rare:102 | ||||
| chr4:128811053-128811341 | Rare:60 | ||||
| chr4:129093505-129093741 | Rare:71 | ||||
| chr4:133149105-133149294 | Common:2; Rare:53 | ||||
| chr4:137532455-137532704 | Common:1; Rare:41 | ||||
| chr4:139084192-139084302 | Rare:47 | ||||
| chr4:139177192-139177456 | Rare:78 | ||||
| chr4:139301184-139301557 | Common:6; Rare:104 | ||||
| chr4:139453683-139453749 | Common:2; Rare:21 | ||||
| chr4:139453770-139454265 | Common:3; Rare:141; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556115-139556264 | Rare:32 | ||||
| chr4:139556281-139556557 | Rare:52 |