| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30246313-30246715 | Common:2; Rare:106 | ||||
| chr22:30246746-30246933 | Rare:43 | ||||
| chr22:30326850-30327205 | Common:3; Rare:126 | ||||
| chr22:30356740-30357049 | Common:2; Rare:100 | ||||
| chr22:30387337-30387671 | Common:6; Rare:105 | ||||
| chr22:30579751-30580180 | Common:2; Rare:127 | ||||
| chr22:30606805-30606863 | Rare:24 | ||||
| chr22:30607045-30607244 | Common:3; Rare:61; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:30635450-30635789 | Common:8; Rare:101 | ||||
| chr22:30967902-30967984 | Rare:23 | ||||
| chr22:30967989-30968070 | Rare:23 | ||||
| chr22:30968159-30968501 | Common:1; Rare:84 | ||||
| chr22:31081265-31081425 | Common:1; Rare:57 | ||||
| chr22:31088454-31088776 | Rare:102 | ||||
| chr22:31160092-31160299 | Common:1; Rare:70 |