| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34516331-34516446 | Rare:44 | ||||
| chr20:34677086-34677325 | Rare:60 | ||||
| chr20:34955741-34955922 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35147306-35147386 | Rare:22 | ||||
| chr20:35284733-35284870 | Common:1; Rare:48 | ||||
| chr20:35455059-35455311 | Common:1; Rare:88 | ||||
| chr20:35541926-35542100 | Common:2; Rare:72 | ||||
| chr20:35664867-35665012 | Common:1; Rare:38 | ||||
| chr20:35699329-35699637 | Rare:91 | ||||
| chr20:35742182-35742670 | Common:6; Rare:161 | ||||
| chr20:36236364-36236485 | Common:2; Rare:30 | ||||
| chr20:36746059-36746297 | Common:2; Rare:85 | ||||
| chr20:37095939-37096244 | Common:1; Rare:103 | ||||
| chr20:37178865-37179156 | Rare:83 | ||||
| chr20:37527850-37528175 | Common:4; Rare:108 |