| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35664880-35665027 | Common:1; Rare:36 | ||||
| chr20:35699190-35699260 | Rare:9 | ||||
| chr20:35699284-35699587 | Rare:90; Clinvar (benign):3 | ||||
| chr20:35742175-35742689 | Common:6; Rare:172 | ||||
| chr20:36236419-36236491 | Rare:15 | ||||
| chr20:36573383-36573497 | Rare:41 | ||||
| chr20:36605495-36605796 | Common:2; Rare:105 | ||||
| chr20:36746062-36746304 | Common:2; Rare:87 | ||||
| chr20:36773724-36774003 | Common:3; Rare:87 | ||||
| chr20:36951650-36951922 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:37095939-37096018 | Rare:35 | ||||
| chr20:37178865-37179231 | Rare:108 | ||||
| chr20:37289605-37289682 | Common:1; Rare:28 | ||||
| chr20:37527834-37528125 | Common:3; Rare:100 | ||||
| chr20:38033415-38033775 | Common:2; Rare:105 |