| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34558501-34558731 | Common:1; Rare:58 | ||||
| chr20:34677086-34677331 | Rare:62 | ||||
| chr20:34872821-34872903 | Rare:32 | ||||
| chr20:34955741-34955868 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35147302-35147381 | Rare:23 | ||||
| chr20:35284728-35284829 | Common:1; Rare:35 | ||||
| chr20:35411953-35412087 | Rare:50 | ||||
| chr20:35556043-35556266 | Rare:69 | ||||
| chr20:35556712-35556987 | Common:2; Rare:67 | ||||
| chr20:35664880-35665047 | Common:1; Rare:42 | ||||
| chr20:35699190-35699475 | Rare:82; Clinvar (benign):3 | ||||
| chr20:35740822-35741167 | Common:3; Rare:90 | ||||
| chr20:35742097-35742649 | Common:5; Rare:176 | ||||
| chr20:35771854-35772077 | Common:2; Rare:72 | ||||
| chr20:36236180-36236500 | Common:2; Rare:61 |