| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801205-121801397 | Common:3; Rare:73 | ||||
| chr4:121823851-121824147 | Common:2; Rare:77 | ||||
| chr4:121870369-121870737 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr4:122152207-122152461 | Common:2; Rare:100 | ||||
| chr4:122732354-122732824 | Common:4; Rare:149; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122826576-122826866 | Common:2; Rare:111 | ||||
| chr4:122922000-122922136 | Common:3; Rare:28 | ||||
| chr4:122922556-122922672 | Common:2; Rare:56 | ||||
| chr4:122922945-122923186 | Common:2; Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396669-123396806 | Rare:29 | ||||
| chr4:123397010-123397640 | Common:2; Rare:182 | ||||
| chr4:123397639-123398291 | Common:6; Rare:212 | ||||
| chr4:123398193-123398835 | Common:7; Rare:369 | ||||
| chr4:123398849-123399653 | Common:18; Rare:346 | ||||
| chr4:124712108-124712259 | Rare:32 |