| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3795691-3795845 | Common:2; Rare:41 | ||||
| chr20:3796124-3796545 | Common:4; Rare:95 | ||||
| chr20:3846741-3846893 | Rare:44 | ||||
| chr20:3889064-3889423 | Common:2; Rare:204; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr20:4015471-4015764 | Common:4; Rare:104 | ||||
| chr20:4148562-4148934 | Rare:101 | ||||
| chr20:4686212-4686511 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:5112874-5113171 | Common:1; Rare:115 | ||||
| chr20:5119811-5120179 | Common:1; Rare:124 | ||||
| chr20:5126538-5126852 | Common:3; Rare:91 | ||||
| chr20:5610879-5611247 | Common:3; Rare:134 | ||||
| chr20:5950307-5950707 | Common:8; Rare:121 | ||||
| chr20:6005826-6006131 | Common:2; Rare:85 | ||||
| chr20:6006211-6006548 | Common:3; Rare:96 | ||||
| chr20:6028031-6028273 | Rare:52 |