| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:19758021-19758289 | Common:4; Rare:91 | ||||
| chr20:23048630-23048854 | Rare:81; Clinvar:5 | ||||
| chr20:23084435-23084687 | Common:1; Rare:98 | ||||
| chr20:23084744-23085085 | Common:3; Rare:131 | ||||
| chr20:23087168-23087440 | Common:2; Rare:51 | ||||
| chr20:24964013-24964037 | Rare:9 | ||||
| chr20:25281734-25282060 | Common:5; Rare:73 | ||||
| chr20:25292155-25292536 | Common:5; Rare:137; Clinvar (pathogenic):1 | ||||
| chr20:25853981-25854116 | Common:3; Rare:49 | ||||
| chr20:29497229-29497403 | |||||
| chr20:31604327-31604444 | Rare:45 | ||||
| chr20:36050322-36050732 | Common:2; Rare:142 | ||||
| chr20:38139469-38139845 | Common:1; Rare:99 | ||||
| chr20:44055179-44055353 | Common:1; Rare:27 | ||||
| chr20:44618082-44618341 | Common:4; Rare:48 |