| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628637-17628866 | Common:2; Rare:79 | ||||
| chr22:17638647-17638830 | Rare:69 | ||||
| chr22:17706615-17706810 | Common:1; Rare:42 | ||||
| chr22:18024311-18024641 | Common:1; Rare:83 | ||||
| chr22:18077814-18078028 | Common:4; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18150037-18150179 | Common:1; Rare:39 | ||||
| chr22:19122389-19122650 | Common:3; Rare:60 | ||||
| chr22:19178447-19178527 | Common:1; Rare:20 | ||||
| chr22:19291683-19291988 | Common:10; Rare:108 | ||||
| chr22:19432303-19432610 | Common:4; Rare:131 | ||||
| chr22:19447677-19447771 | Common:1; Rare:46 | ||||
| chr22:19479112-19479475 | Common:4; Rare:131 | ||||
| chr22:19479687-19479960 | Common:4; Rare:76 | ||||
| chr22:19854791-19855033 | Rare:91 | ||||
| chr22:19941715-19941881 | Rare:70; Clinvar:5; Clinvar (benign):4 |