| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50958461-50958830 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:53593790-53593894 | Common:1; Rare:38 | ||||
| chr20:58309431-58309715 | Common:2; Rare:111 | ||||
| chr20:58388977-58389275 | Common:3; Rare:132; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651113-58651306 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58652040-58652105 | Rare:15 | ||||
| chr20:58981156-58981318 | Common:2; Rare:83 | ||||
| chr20:59042763-59043063 | Common:1; Rare:112 | ||||
| chr20:59933594-59933792 | Common:4; Rare:80 | ||||
| chr20:59940246-59940474 | Rare:91 | ||||
| chr20:62143299-62143812 | Common:6; Rare:219 | ||||
| chr20:62182917-62183049 | Rare:46 | ||||
| chr20:62386946-62387136 | Common:3; Rare:84 | ||||
| chr20:62937867-62938199 | Common:2; Rare:124 | ||||
| chr20:63272729-63272863 | Common:1; Rare:41 |