| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:3071988-3072175 | Rare:44 | ||||
| chr20:3159809-3159934 | Rare:43 | ||||
| chr20:3173521-3173650 | Common:1; Rare:49 | ||||
| chr20:3209429-3209535 | Common:1; Rare:33 | ||||
| chr20:3407555-3407722 | Common:3; Rare:46 | ||||
| chr20:3407906-3408024 | Rare:31 | ||||
| chr20:3470876-3471091 | Common:2; Rare:115 | ||||
| chr20:3767730-3767917 | Common:2; Rare:56 | ||||
| chr20:3796202-3796545 | Common:4; Rare:75 | ||||
| chr20:3820442-3820582 | Common:1; Rare:59 | ||||
| chr20:3846560-3846901 | Common:4; Rare:85 | ||||
| chr20:3888838-3888933 | Rare:23 | ||||
| chr20:3889157-3889412 | Common:1; Rare:134; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:5112861-5113168 | Common:1; Rare:114 | ||||
| chr20:5119913-5120174 | Common:1; Rare:88 |