| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40951015-40951413 | Common:2; Rare:137 | ||||
| chr22:40951600-40951725 | Common:1; Rare:35 | ||||
| chr22:41091406-41091847 | Common:6; Rare:164 | ||||
| chr22:41286152-41286557 | Common:2; Rare:128 | ||||
| chr22:41367133-41367465 | Rare:94 | ||||
| chr22:41446411-41446450 | Common:1; Rare:10 | ||||
| chr22:41446491-41446542 | Rare:8 | ||||
| chr22:41446756-41446958 | Rare:82 | ||||
| chr22:41468633-41469175 | Common:2; Rare:152 | ||||
| chr22:41515219-41515506 | Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:41544593-41544871 | Common:4; Rare:65 | ||||
| chr22:41620698-41620766 | Rare:21 | ||||
| chr22:41621000-41621384 | Common:7; Rare:139 | ||||
| chr22:41800506-41800688 | Common:1; Rare:58 | ||||
| chr22:41832909-41833354 | Common:3; Rare:148 |