| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62926469-62926578 | Common:2; Rare:39 | ||||
| chr20:62937879-62938194 | Common:2; Rare:116 | ||||
| chr20:62952588-62952808 | Common:3; Rare:58 | ||||
| chr20:62952812-62953083 | Common:3; Rare:85; Clinvar (pathogenic):1 | ||||
| chr20:63272663-63272894 | Common:5; Rare:82 | ||||
| chr20:63574215-63574323 | Rare:26 | ||||
| chr20:63626972-63627251 | Rare:111 | ||||
| chr20:63653359-63653633 | Common:2; Rare:33 | ||||
| chr20:63658241-63658349 | Common:2; Rare:33 | ||||
| chr20:63707846-63708118 | Rare:80 | ||||
| chr20:63865066-63865368 | Common:2; Rare:116 | ||||
| chr20:63980969-63981260 | Common:4; Rare:93; Clinvar:7; Clinvar (benign):4 | ||||
| chr20:64062941-64063284 | Common:3; Rare:124 | ||||
| chr20:64079924-64080091 | Common:1; Rare:72 | ||||
| chr21:14383110-14383486 | Common:2; Rare:106 |