| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18467332-18467464 | Common:2; Rare:27 | ||||
| chr20:18507384-18507624 | Common:1; Rare:66; Clinvar:1 | ||||
| chr20:18567308-18567530 | Common:2; Rare:80 | ||||
| chr20:19889289-19889539 | Common:2; Rare:43 | ||||
| chr20:19935032-19935126 | Common:2; Rare:31; Clinvar (benign):2 | ||||
| chr20:19935293-19935493 | Rare:31 | ||||
| chr20:20017147-20017420 | Rare:89 | ||||
| chr20:20018085-20018125 | Rare:7 | ||||
| chr20:20038421-20038712 | Common:1; Rare:56 | ||||
| chr20:21303261-21303470 | Rare:71 | ||||
| chr20:23049651-23049806 | Common:3; Rare:48; Clinvar (pathogenic):1 | ||||
| chr20:23086310-23086452 | Rare:22 | ||||
| chr20:23350522-23350882 | Common:2; Rare:109 | ||||
| chr20:23361843-23362228 | Common:3; Rare:131 | ||||
| chr20:23421389-23421629 | Common:4; Rare:106 |