| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34677074-34677318 | Rare:64 | ||||
| chr20:34955741-34955928 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr20:35147273-35147416 | Common:1; Rare:50 | ||||
| chr20:35171840-35172114 | Rare:49 | ||||
| chr20:35278034-35278227 | Common:5; Rare:69 | ||||
| chr20:35279565-35279897 | Common:1; Rare:85 | ||||
| chr20:35284696-35284954 | Common:2; Rare:74 | ||||
| chr20:35292325-35292657 | Common:2; Rare:76 | ||||
| chr20:35455040-35455311 | Common:1; Rare:91 | ||||
| chr20:35664876-35664981 | Common:1; Rare:31 | ||||
| chr20:35699264-35699662 | Rare:124; Clinvar (benign):3 | ||||
| chr20:35740804-35741121 | Common:3; Rare:94 | ||||
| chr20:35741939-35742657 | Common:6; Rare:235 | ||||
| chr20:36472893-36473097 | Common:1; Rare:33 | ||||
| chr20:36573247-36573475 | Common:1; Rare:80 |