Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41446778-41446945 | Rare:64 | ||||
chr22:41468651-41468751 | Common:2; Rare:33 | ||||
chr22:41469015-41469159 | Rare:53 | ||||
chr22:41560927-41561127 | Common:9; Rare:61 | ||||
chr22:41621000-41621380 | Common:7; Rare:138 | ||||
chr22:41800517-41800669 | Rare:51 | ||||
chr22:41832909-41833221 | Common:3; Rare:104 | ||||
chr22:41833238-41833355 | Rare:35 | ||||
chr22:42070766-42070948 | Common:2; Rare:40 | ||||
chr22:42079495-42079861 | Common:2; Rare:114 | ||||
chr22:42090607-42091001 | Common:2; Rare:167; Clinvar (pathogenic):1 | ||||
chr22:42210690-42210924 | Rare:76 | ||||
chr22:42614811-42615250 | Common:4; Rare:194 | ||||
chr22:42649310-42649482 | Common:1; Rare:67 | ||||
chr22:42856731-42857046 | Common:2; Rare:89 |