| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35664865-35664993 | Common:1; Rare:38 | ||||
| chr20:35699181-35699274 | Rare:13 | ||||
| chr20:35699298-35699497 | Rare:68; Clinvar (benign):3 | ||||
| chr20:35742097-35742666 | Common:6; Rare:183 | ||||
| chr20:35771824-35772055 | Common:2; Rare:74 | ||||
| chr20:36236323-36236530 | Common:2; Rare:55 | ||||
| chr20:36461133-36461498 | Common:1; Rare:107 | ||||
| chr20:36573388-36573597 | Rare:88 | ||||
| chr20:36746055-36746304 | Common:2; Rare:89 | ||||
| chr20:36773755-36773918 | Common:2; Rare:52 | ||||
| chr20:36951623-36951924 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:37178865-37179225 | Rare:107 | ||||
| chr20:37179519-37179623 | Common:1; Rare:39 | ||||
| chr20:37289578-37289723 | Common:2; Rare:57 | ||||
| chr20:37521077-37521397 | Common:1; Rare:87 |