| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40953307-40953657 | Common:1; Rare:66 | ||||
| chr22:40961110-40961167 | Rare:8 | ||||
| chr22:41064590-41064692 | Rare:15 | ||||
| chr22:41073625-41073880 | Common:2; Rare:43 | ||||
| chr22:41092484-41092622 | Rare:72 | ||||
| chr22:41092757-41093054 | Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:41097166-41097394 | Common:2; Rare:42 | ||||
| chr22:41160494-41160714 | Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:41197422-41197653 | Common:2; Rare:63 | ||||
| chr22:41256018-41256293 | Common:1; Rare:86 | ||||
| chr22:41268100-41268443 | Common:1; Rare:84 | ||||
| chr22:41302227-41302548 | Common:2; Rare:74 | ||||
| chr22:41302585-41302879 | Common:1; Rare:67 | ||||
| chr22:41311091-41311217 | Rare:19 | ||||
| chr22:41325570-41325828 | Rare:66 |