| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18524770-18524981 | Common:1; Rare:46; Clinvar (pathogenic):1 | ||||
| chr20:18705562-18705733 | Common:1; Rare:33 | ||||
| chr20:18793954-18794096 | Rare:47 | ||||
| chr20:19757959-19758258 | Common:4; Rare:108 | ||||
| chr20:19884865-19885014 | Common:2; Rare:31 | ||||
| chr20:19885276-19885388 | Common:4; Rare:15 | ||||
| chr20:19977107-19977270 | Common:1; Rare:41 | ||||
| chr20:19994101-19994195 | Rare:14 | ||||
| chr20:21436313-21436572 | Common:1; Rare:48 | ||||
| chr20:25751078-25751215 | Rare:33 | ||||
| chr20:28602692-28602887 | |||||
| chr20:29080172-29080281 | |||||
| chr20:29497184-29497403 | |||||
| chr20:30377054-30377308 | Common:8; Rare:32 | ||||
| chr20:30579939-30580219 | Common:1; Rare:53 |