Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:109334078-109334385 | Common:1; Rare:75 | ||||
chr8:117520581-117520749 | Common:4; Rare:34 | ||||
chr8:124539058-124539278 | Common:1; Rare:104; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr8:143018412-143018566 | Common:1; Rare:45 | ||||
chr8:143558269-143558390 | Common:1; Rare:47 | ||||
chr9:6015603-6015721 | Rare:50 | ||||
chr9:18473964-18474163 | Rare:50 | ||||
chr9:21994928-21995095 | Common:1; Rare:28 | ||||
chr9:33025112-33025285 | Common:5; Rare:68 | ||||
chr9:33264917-33265060 | Rare:42 | ||||
chr9:33290366-33290538 | Common:2; Rare:61 | ||||
chr9:35732161-35732676 | Common:3; Rare:137 | ||||
chr9:83980623-83980778 | Common:2; Rare:59 | ||||
chr9:92325339-92325653 | Common:4; Rare:72 | ||||
chr9:97633312-97633605 | Common:3; Rare:88 |