Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:38681810-38682035 | Common:2; Rare:97 | ||||
chr22:39014208-39014298 | Rare:24 | ||||
chr22:39319601-39319826 | Common:3; Rare:95 | ||||
chr22:39349801-39349998 | Common:1; Rare:63 | ||||
chr22:40346409-40346556 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr22:40636686-40637031 | Common:2; Rare:93 | ||||
chr22:40856926-40857154 | Common:1; Rare:91; Clinvar:3 | ||||
chr22:41286167-41286472 | Common:2; Rare:93 | ||||
chr22:41469022-41469141 | Rare:38 | ||||
chr22:41560903-41561125 | Common:9; Rare:65 | ||||
chr22:41620998-41621370 | Common:7; Rare:136 | ||||
chr22:41800579-41800688 | Common:1; Rare:30 | ||||
chr22:41832915-41833221 | Common:3; Rare:101 | ||||
chr22:41947114-41947265 | Rare:50 | ||||
chr22:42070782-42070961 | Common:2; Rare:36 |