| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2664151-2664273 | Common:2; Rare:54; Clinvar:1 | ||||
| chr20:2755117-2755360 | Rare:37 | ||||
| chr20:2800558-2800804 | Common:1; Rare:71 | ||||
| chr20:2840604-2840771 | Common:1; Rare:65 | ||||
| chr20:3173521-3173718 | Common:1; Rare:67 | ||||
| chr20:3208642-3208829 | Rare:26 | ||||
| chr20:3209425-3209694 | Common:1; Rare:94; Clinvar:1 | ||||
| chr20:3221774-3221918 | Rare:52; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr20:3470923-3471077 | Common:1; Rare:72 | ||||
| chr20:3767719-3767992 | Common:3; Rare:86 | ||||
| chr20:3786757-3786997 | Common:3; Rare:73 | ||||
| chr20:3796032-3796550 | Common:4; Rare:115 | ||||
| chr20:3888690-3888868 | Common:1; Rare:41 | ||||
| chr20:3889041-3889423 | Common:2; Rare:218; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr20:3889762-3889878 | Common:2; Rare:51 |