| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37562731-37562793 | Common:1; Rare:20 | ||||
| chr22:37633551-37633753 | Common:1; Rare:46 | ||||
| chr22:37747393-37747687 | Common:1; Rare:62 | ||||
| chr22:37765432-37765815 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:37768836-37769086 | Common:1; Rare:69; Clinvar (pathogenic):1 | ||||
| chr22:37805919-37806150 | Common:1; Rare:74 | ||||
| chr22:37806159-37806420 | Common:3; Rare:53 | ||||
| chr22:37816252-37816539 | Common:1; Rare:71 | ||||
| chr22:37863009-37863336 | Common:1; Rare:81 | ||||
| chr22:38203949-38204055 | Common:1; Rare:19 | ||||
| chr22:38314508-38314734 | Common:1; Rare:47 | ||||
| chr22:38683634-38683811 | Rare:46 | ||||
| chr22:38745771-38745978 | Rare:53 | ||||
| chr22:39521625-39521732 | Rare:52 | ||||
| chr22:40362949-40363022 | Rare:25; Clinvar:1; Clinvar (benign):2 |