Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:75368585-75368832 | Rare:68 | ||||
chr15:75455801-75455967 | Rare:52 | ||||
chr15:75625532-75625823 | Common:2; Rare:68 | ||||
chr15:75647572-75647950 | Common:2; Rare:92 | ||||
chr15:75647969-75648201 | Rare:51 | ||||
chr15:75649886-75650019 | Rare:33 | ||||
chr15:75843332-75843687 | Common:1; Rare:140 | ||||
chr15:75903835-75903961 | Rare:54 | ||||
chr15:76012374-76012433 | Rare:9 | ||||
chr15:76286370-76286687 | Common:3; Rare:73; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr15:76311349-76311609 | Common:1; Rare:89; Clinvar:7; Clinvar (benign):8 | ||||
chr15:76576900-76577132 | Common:1; Rare:43 | ||||
chr15:77420057-77420433 | Common:2; Rare:105 | ||||
chr15:78092408-78092572 | Common:1; Rare:41 | ||||
chr15:78149176-78149418 | Common:1; Rare:81 |