Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:67254629-67254824 | Rare:68 | ||||
chr15:67542613-67542756 | Common:2; Rare:48 | ||||
chr15:69414268-69414372 | Rare:32 | ||||
chr15:70892499-70892823 | Common:1; Rare:64 | ||||
chr15:72118167-72118417 | Common:2; Rare:78 | ||||
chr15:72231115-72231523 | Common:3; Rare:131 | ||||
chr15:73633344-73633595 | Common:2; Rare:87 | ||||
chr15:73926288-73926486 | Rare:51 | ||||
chr15:73994595-73994767 | Rare:34 | ||||
chr15:74202430-74202546 | Rare:21 | ||||
chr15:74202770-74202983 | Rare:53; Clinvar:2 | ||||
chr15:74540966-74541276 | Common:4; Rare:109 | ||||
chr15:74873299-74873488 | Common:6; Rare:58 | ||||
chr15:74889867-74890076 | Rare:65; Clinvar (pathogenic):1 | ||||
chr15:75201660-75201908 | Rare:64 |