| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40044434-40044865 | Common:2; Rare:102 | ||||
| chr22:40045299-40045542 | Common:2; Rare:60 | ||||
| chr22:40177685-40177990 | Rare:88 | ||||
| chr22:40178313-40178570 | Rare:53 | ||||
| chr22:40345935-40346085 | Rare:34 | ||||
| chr22:40346232-40346857 | Common:3; Rare:228; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr22:40370433-40370793 | Common:1; Rare:126 | ||||
| chr22:40370853-40371056 | Rare:44 | ||||
| chr22:40436644-40436899 | Rare:52 | ||||
| chr22:40463388-40463552 | Rare:28 | ||||
| chr22:40533812-40533971 | Rare:39 | ||||
| chr22:40636340-40636496 | Rare:58 | ||||
| chr22:40636617-40637087 | Common:3; Rare:134 | ||||
| chr22:40818869-40818992 | Common:1; Rare:35 | ||||
| chr22:40819264-40819588 | Common:11; Rare:139 |