| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:222319028-222319313 | Common:1; Rare:54 | ||||
| chr2:226796876-226797121 | Rare:78; Clinvar (pathogenic):1 | ||||
| chr20:3785011-3785083 | Rare:22 | ||||
| chr20:19757528-19757663 | Common:2; Rare:38 | ||||
| chr20:19757945-19758266 | Common:4; Rare:110 | ||||
| chr20:19784714-19784870 | Rare:25 | ||||
| chr20:20088589-20088858 | Common:6; Rare:44 | ||||
| chr20:23358114-23358247 | Common:1; Rare:39 | ||||
| chr20:23633500-23633709 | Common:2; Rare:49 | ||||
| chr20:34096756-34096990 | Rare:45 | ||||
| chr20:36050329-36050737 | Common:1; Rare:144 | ||||
| chr20:37988886-37988920 | Rare:5 | ||||
| chr20:41116041-41116357 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
| chr20:45419361-45419539 | Common:1; Rare:74; Clinvar (pathogenic):1 | ||||
| chr20:47352575-47352698 | Rare:20 |