| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47352310-47352695 | Common:1; Rare:66 | ||||
| chr20:47356666-47356887 | Rare:51 | ||||
| chr20:49278030-49278272 | Rare:65 | ||||
| chr20:49568045-49568157 | Common:2; Rare:27 | ||||
| chr20:49812573-49812925 | Common:2; Rare:81 | ||||
| chr20:49915487-49915602 | Common:3; Rare:40 | ||||
| chr20:50113106-50113244 | Common:5; Rare:69 | ||||
| chr20:50131122-50131269 | Common:1; Rare:20 | ||||
| chr20:50958487-50958843 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:56392197-56392688 | Common:6; Rare:128 | ||||
| chr20:56468551-56468705 | Rare:70 | ||||
| chr20:57266078-57266432 | Common:1; Rare:80 | ||||
| chr20:58309428-58309715 | Common:2; Rare:113 | ||||
| chr20:58389007-58389277 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:58651080-58651305 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 |