| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44600226-44600454 | Rare:34 | ||||
| chr20:44610639-44610707 | Rare:16 | ||||
| chr20:44896555-44896667 | Rare:20 | ||||
| chr20:44952482-44952668 | Rare:29 | ||||
| chr20:44959353-44959366 | Rare:3 | ||||
| chr20:44977319-44977368 | Common:1; Rare:7 | ||||
| chr20:45820287-45820345 | Rare:12 | ||||
| chr20:45904829-45905056 | Rare:78 | ||||
| chr20:45950089-45950272 | Common:3; Rare:57; Clinvar:2 | ||||
| chr20:45957572-45957836 | Rare:73 | ||||
| chr20:45971538-45971638 | Rare:27 | ||||
| chr20:46071728-46072010 | Rare:54 | ||||
| chr20:46088923-46089153 | Common:1; Rare:46 | ||||
| chr20:46123177-46123472 | Rare:57; Clinvar:1 | ||||
| chr20:46353870-46354045 | Rare:27 |