| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35399904-35400208 | Rare:106 | ||||
| chr22:35648288-35648530 | Common:2; Rare:36 | ||||
| chr22:35840381-35840669 | Common:1; Rare:66 | ||||
| chr22:36387922-36388348 | Common:3; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481567-36481729 | Common:2; Rare:45 | ||||
| chr22:36481968-36482236 | Common:2; Rare:70 | ||||
| chr22:36507038-36507191 | Common:3; Rare:58 | ||||
| chr22:36529067-36529568 | Common:8; Rare:158 | ||||
| chr22:36860865-36861069 | Rare:38 | ||||
| chr22:37199367-37199554 | Common:2; Rare:49 | ||||
| chr22:37244153-37244339 | Rare:54 | ||||
| chr22:37484522-37484775 | Common:2; Rare:70 | ||||
| chr22:37486341-37486534 | Common:1; Rare:59 | ||||
| chr22:37608679-37608881 | Common:1; Rare:59 | ||||
| chr22:37608911-37609059 | Common:1; Rare:44 |