| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121823835-121824070 | Common:2; Rare:58 | ||||
| chr4:121870406-121870583 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr4:122152272-122152410 | Common:2; Rare:58 | ||||
| chr4:122732523-122732768 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922922-122923182 | Common:2; Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396681-123396817 | Rare:33 | ||||
| chr4:124712566-124713057 | Common:1; Rare:139 | ||||
| chr4:127880784-127880929 | Rare:51 | ||||
| chr4:128060994-128061401 | Common:1; Rare:137 | ||||
| chr4:128287960-128288285 | Common:5; Rare:94 | ||||
| chr4:128811233-128811313 | Rare:18 | ||||
| chr4:129093458-129093748 | Common:1; Rare:85 | ||||
| chr4:133149066-133149329 | Common:2; Rare:78 | ||||
| chr4:139177091-139177456 | Rare:100 | ||||
| chr4:139301291-139301616 | Common:4; Rare:99 |