| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:28741800-28742078 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28742402-28742701 | Common:1; Rare:73 | ||||
| chr22:28800345-28800702 | Common:5; Rare:128 | ||||
| chr22:29267835-29268348 | Common:2; Rare:150 | ||||
| chr22:29553537-29553809 | Rare:81 | ||||
| chr22:29581078-29581211 | Common:2; Rare:41 | ||||
| chr22:29603591-29603764 | Common:1; Rare:42; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:29767032-29767440 | Common:4; Rare:129 | ||||
| chr22:30356785-30356994 | Common:1; Rare:71 | ||||
| chr22:30607104-30607325 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:31081167-31081371 | Common:1; Rare:55 | ||||
| chr22:31107461-31107708 | Common:2; Rare:82 | ||||
| chr22:31399480-31399658 | Rare:53 | ||||
| chr22:31630795-31631038 | Common:5; Rare:60 | ||||
| chr22:31753822-31753987 | Rare:57 |