Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7557923-7558119 | Common:3; Rare:50 | ||||
chr17:7558148-7558340 | Common:1; Rare:38 | ||||
chr17:7561773-7562065 | Common:3; Rare:82 | ||||
chr17:7573900-7573978 | Rare:26 | ||||
chr17:7577068-7577566 | Common:1; Rare:137 | ||||
chr17:7583510-7583916 | Common:1; Rare:161; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:7584057-7584099 | Rare:14 | ||||
chr17:7589978-7590355 | Rare:73 | ||||
chr17:7627454-7627596 | Common:1; Rare:42 | ||||
chr17:7627740-7627994 | Common:3; Rare:84 | ||||
chr17:7650723-7650934 | Common:2; Rare:59 | ||||
chr17:7686413-7686701 | Rare:71 | ||||
chr17:7687428-7687572 | Rare:37; Clinvar:2 | ||||
chr17:7857162-7857416 | Common:2; Rare:127 | ||||
chr17:7857467-7857746 | Common:2; Rare:89 |