| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39502072-39502459 | Rare:290 | ||||
| chr22:39519368-39519756 | Rare:175 | ||||
| chr22:39519883-39520658 | Common:8; Rare:569 | ||||
| chr22:39520986-39521245 | Common:7; Rare:164 | ||||
| chr22:39532652-39533163 | Common:7; Rare:441 | ||||
| chr22:40044090-40044413 | Common:6; Rare:200 | ||||
| chr22:40044485-40044946 | Common:7; Rare:271 | ||||
| chr22:40044977-40045463 | Common:6; Rare:226 | ||||
| chr22:40177722-40177999 | Rare:151 | ||||
| chr22:40345994-40346100 | Rare:21 | ||||
| chr22:40346201-40346602 | Common:2; Rare:292; Clinvar:13; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr22:40346620-40346940 | Common:4; Rare:149; Clinvar:4; Clinvar (benign):7 | ||||
| chr22:40370474-40370732 | Rare:92 | ||||
| chr22:40370706-40371320 | Common:4; Rare:241 | ||||
| chr22:40403588-40404429 | Common:8; Rare:352 |