| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35664867-35665012 | Common:1; Rare:38 | ||||
| chr20:35699298-35699456 | Rare:52; Clinvar (benign):3 | ||||
| chr20:35741618-35741660 | Common:1; Rare:13 | ||||
| chr20:35742165-35742617 | Common:5; Rare:138 | ||||
| chr20:35771784-35772055 | Common:2; Rare:81 | ||||
| chr20:36541296-36541603 | Common:3; Rare:84 | ||||
| chr20:36573246-36573622 | Common:1; Rare:156 | ||||
| chr20:36746044-36746297 | Common:2; Rare:92 | ||||
| chr20:36951436-36951532 | Rare:23; Clinvar (benign):1 | ||||
| chr20:36951534-36951896 | Common:1; Rare:125; Clinvar:3; Clinvar (benign):5 | ||||
| chr20:37178865-37179217 | Rare:104 | ||||
| chr20:37289577-37289677 | Common:1; Rare:33 | ||||
| chr20:37345960-37346150 | Rare:51 | ||||
| chr20:38033419-38033813 | Common:2; Rare:116 | ||||
| chr20:38260692-38261040 | Common:2; Rare:87 |