| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3820040-3820960 | Common:11; Rare:629 | ||||
| chr20:3846589-3846948 | Common:7; Rare:235 | ||||
| chr20:3847243-3847470 | Rare:93 | ||||
| chr20:3888193-3888459 | Common:3; Rare:63 | ||||
| chr20:3888748-3888929 | Rare:47 | ||||
| chr20:3888968-3889488 | Common:10; Rare:750; Clinvar:27; Clinvar (benign):15; Clinvar (pathogenic):6 | ||||
| chr20:3889660-3889910 | Common:12; Rare:199; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:4015337-4015784 | Common:13; Rare:327 | ||||
| chr20:4148600-4148884 | Rare:191 | ||||
| chr20:4172070-4172420 | Common:2; Rare:70 | ||||
| chr20:4686245-4686521 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:4823468-4823709 | Common:1; Rare:48 | ||||
| chr20:5001423-5001673 | Common:1; Rare:70 | ||||
| chr20:5112826-5113276 | Common:4; Rare:394 | ||||
| chr20:5119270-5119640 | Common:8; Rare:316 |