| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:46689291-46689893 | Common:3; Rare:175 | ||||
| chr20:46894610-46894679 | Rare:26 | ||||
| chr20:46894710-46894855 | Rare:50 | ||||
| chr20:47355961-47356084 | Common:1; Rare:20 | ||||
| chr20:47356661-47356988 | Rare:78 | ||||
| chr20:47357173-47357562 | Rare:78 | ||||
| chr20:47501681-47502163 | Common:2; Rare:160 | ||||
| chr20:47784810-47785007 | Rare:43 | ||||
| chr20:48827883-48828466 | Common:6; Rare:181 | ||||
| chr20:48921530-48921873 | Common:4; Rare:135; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:48922014-48922147 | Rare:43 | ||||
| chr20:49046062-49046371 | Common:4; Rare:85 | ||||
| chr20:49046588-49046967 | Common:4; Rare:127 | ||||
| chr20:49188232-49188613 | Common:3; Rare:138 | ||||
| chr20:49219173-49219529 | Common:1; Rare:147 |