| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:33993048-33993443 | Common:2; Rare:182 | ||||
| chr20:33993453-33994130 | Common:6; Rare:405 | ||||
| chr20:33994320-33994642 | Common:3; Rare:145 | ||||
| chr20:34075954-34077450 | Common:19; Rare:739 | ||||
| chr20:34111718-34111951 | Rare:89 | ||||
| chr20:34112083-34112540 | Common:2; Rare:307 | ||||
| chr20:34302908-34303183 | Rare:142 | ||||
| chr20:34303197-34303596 | Common:6; Rare:293; Clinvar:9; Clinvar (benign):7 | ||||
| chr20:34363100-34363377 | Rare:139 | ||||
| chr20:34363440-34363904 | Common:1; Rare:192 | ||||
| chr20:34516249-34516505 | Common:10; Rare:264 | ||||
| chr20:34516510-34516850 | Common:1; Rare:167 | ||||
| chr20:34676410-34676954 | Common:3; Rare:201 | ||||
| chr20:34677032-34677403 | Rare:254 | ||||
| chr20:34704097-34704392 | Common:3; Rare:225 |