Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:74461094-74461338 | Rare:72 | ||||
chr15:74540966-74541293 | Common:4; Rare:118 | ||||
chr15:74598381-74598511 | Common:1; Rare:52 | ||||
chr15:74614659-74614965 | Common:3; Rare:95 | ||||
chr15:74615492-74615891 | Common:4; Rare:121 | ||||
chr15:74627213-74627446 | Common:2; Rare:47 | ||||
chr15:74695946-74696064 | Rare:39 | ||||
chr15:74781916-74782126 | Common:3; Rare:70 | ||||
chr15:74821030-74821138 | Rare:32 | ||||
chr15:74843087-74843329 | Common:2; Rare:76 | ||||
chr15:74872928-74873109 | Rare:39 | ||||
chr15:74889707-74890076 | Rare:97; Clinvar (pathogenic):1 | ||||
chr15:74906781-74906871 | Common:1; Rare:41 | ||||
chr15:75043149-75043325 | Rare:26 | ||||
chr15:75201758-75201952 | Common:1; Rare:71 |