| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121870385-121870669 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr4:122152235-122152445 | Common:2; Rare:88 | ||||
| chr4:122732432-122732791 | Common:2; Rare:112; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922923-122923162 | Common:2; Rare:75; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396658-123396801 | Rare:31 | ||||
| chr4:123399333-123399664 | Common:1; Rare:100 | ||||
| chr4:124712566-124713057 | Common:1; Rare:139 | ||||
| chr4:127622968-127623278 | Common:1; Rare:71 | ||||
| chr4:127632865-127633010 | Rare:39 | ||||
| chr4:127782263-127782402 | Rare:46 | ||||
| chr4:127880784-127880939 | Rare:52 | ||||
| chr4:128060979-128061329 | Common:1; Rare:125 | ||||
| chr4:129093444-129093756 | Common:2; Rare:89 | ||||
| chr4:133149070-133149329 | Common:2; Rare:78 | ||||
| chr4:133154813-133155020 | Common:2; Rare:41 |