| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45935053-45935345 | Rare:112 | ||||
| chr20:45971776-45971897 | Common:2; Rare:45 | ||||
| chr20:46363962-46364064 | Common:1; Rare:18 | ||||
| chr20:46364376-46364538 | Rare:62 | ||||
| chr20:46406565-46406788 | Common:2; Rare:60 | ||||
| chr20:46513541-46513634 | Common:1; Rare:33 | ||||
| chr20:47319034-47319125 | Common:1; Rare:28 | ||||
| chr20:47356664-47356884 | Rare:49 | ||||
| chr20:47501567-47502009 | Common:2; Rare:139 | ||||
| chr20:48921625-48921895 | Common:2; Rare:113; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:49046115-49046354 | Common:3; Rare:70 | ||||
| chr20:49188254-49188612 | Common:3; Rare:128 | ||||
| chr20:49278039-49278272 | Rare:65 | ||||
| chr20:49812731-49812926 | Common:3; Rare:52 | ||||
| chr20:49915496-49915574 | Common:2; Rare:24 |