| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10218716-10218864 | Rare:35 | ||||
| chr20:10434249-10434688 | Common:2; Rare:127 | ||||
| chr20:10640895-10641105 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:11890622-11890897 | Common:2; Rare:99 | ||||
| chr20:11892324-11892471 | Common:2; Rare:28 | ||||
| chr20:13638875-13639035 | Common:1; Rare:49 | ||||
| chr20:13784878-13785116 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:13995259-13995566 | Rare:82 | ||||
| chr20:16573288-16573547 | Common:1; Rare:76 | ||||
| chr20:16729821-16730145 | Common:3; Rare:98 | ||||
| chr20:17569182-17569301 | Rare:23 | ||||
| chr20:17569848-17570208 | Common:5; Rare:139 | ||||
| chr20:17682193-17682620 | Common:5; Rare:140 | ||||
| chr20:17968406-17968614 | Common:4; Rare:89 | ||||
| chr20:17968784-17969150 | Common:3; Rare:127 |