| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:17589555-17589843 | Common:1; Rare:48 | ||||
| chr20:17615988-17616250 | Common:2; Rare:73 | ||||
| chr20:19757478-19757690 | Common:3; Rare:61 | ||||
| chr20:19757945-19758282 | Common:4; Rare:116 | ||||
| chr20:23048807-23048919 | Rare:39; Clinvar:3 | ||||
| chr20:23305120-23305367 | Common:1; Rare:39 | ||||
| chr20:23358119-23358227 | Common:1; Rare:33 | ||||
| chr20:23633406-23633709 | Common:3; Rare:66 | ||||
| chr20:25281890-25282075 | Common:2; Rare:39 | ||||
| chr20:25292241-25292535 | Common:3; Rare:120; Clinvar (pathogenic):1 | ||||
| chr20:25854004-25854118 | Common:3; Rare:43 | ||||
| chr20:28602686-28603139 | |||||
| chr20:30579939-30580248 | Common:2; Rare:57 | ||||
| chr20:31550023-31550091 | Rare:21 | ||||
| chr20:31572905-31573027 | Rare:31 |