Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:30356864-30356985 | Common:1; Rare:40 | ||||
chr22:31160114-31160220 | Common:1; Rare:39 | ||||
chr22:31399495-31399658 | Rare:48 | ||||
chr22:31630802-31630975 | Common:4; Rare:45 | ||||
chr22:31661858-31662012 | Common:2; Rare:44 | ||||
chr22:31662192-31662528 | Common:2; Rare:107 | ||||
chr22:35257383-35257501 | Common:1; Rare:29 | ||||
chr22:35399929-35400199 | Rare:89 | ||||
chr22:37560338-37560509 | Common:1; Rare:59 | ||||
chr22:37849305-37849452 | Rare:87 | ||||
chr22:37953540-37953755 | Common:1; Rare:85 | ||||
chr22:38656369-38656678 | Common:1; Rare:79 | ||||
chr22:38681809-38681979 | Common:1; Rare:70 | ||||
chr22:40346445-40346556 | Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
chr22:40856926-40857154 | Common:1; Rare:91; Clinvar:3 |