| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45935077-45935345 | Rare:102 | ||||
| chr20:46406565-46406781 | Common:2; Rare:55 | ||||
| chr20:47318728-47319139 | Common:2; Rare:131 | ||||
| chr20:47356664-47356872 | Rare:45 | ||||
| chr20:47501764-47502121 | Common:1; Rare:115 | ||||
| chr20:49219282-49219464 | Rare:93 | ||||
| chr20:49278026-49278272 | Rare:66 | ||||
| chr20:49278456-49278717 | Common:9; Rare:101 | ||||
| chr20:49915471-49915602 | Common:3; Rare:49 | ||||
| chr20:50131080-50131268 | Common:1; Rare:28 | ||||
| chr20:50958412-50958851 | Common:1; Rare:159; Clinvar:5; Clinvar (benign):5 | ||||
| chr20:53593803-53593894 | Common:1; Rare:33 | ||||
| chr20:56392197-56392687 | Common:6; Rare:127 | ||||
| chr20:58389861-58390151 | Common:1; Rare:79 | ||||
| chr20:58651080-58651305 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 |