| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35313403-35313651 | Rare:61 | ||||
| chr22:35402873-35403152 | Common:2; Rare:57 | ||||
| chr22:35584169-35584226 | Rare:9 | ||||
| chr22:35744109-35744352 | Rare:58 | ||||
| chr22:35749833-35749915 | Rare:8 | ||||
| chr22:35760971-35761292 | Common:1; Rare:66 | ||||
| chr22:35765272-35765496 | Rare:45 | ||||
| chr22:35836389-35836491 | Rare:27 | ||||
| chr22:35838096-35838273 | Rare:26 | ||||
| chr22:35852297-35852476 | Common:1; Rare:25 | ||||
| chr22:35896400-35896533 | Rare:21 | ||||
| chr22:35902546-35902805 | Common:1; Rare:34 | ||||
| chr22:36025658-36025947 | Common:1; Rare:58 | ||||
| chr22:36279695-36279858 | Common:2; Rare:31 | ||||
| chr22:36286707-36286925 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):7 |