Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94413074-94413169 | Rare:27; Clinvar (pathogenic):1 | ||||
chr7:94420387-94420649 | Rare:72; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr7:95214330-95214618 | Common:3; Rare:46 | ||||
chr7:100335870-100336146 | Common:1; Rare:90 | ||||
chr7:102474773-102474989 | Common:4; Rare:42 | ||||
chr7:102822448-102822472 | Rare:5 | ||||
chr7:105013028-105013199 | Rare:60 | ||||
chr7:105013563-105013673 | Rare:40 | ||||
chr7:112205590-112205679 | Rare:23 | ||||
chr7:113118537-113118671 | Common:1; Rare:44 | ||||
chr7:114419942-114420001 | Rare:5 | ||||
chr7:130511257-130511364 | Rare:20 | ||||
chr7:130520716-130520846 | Rare:19 | ||||
chr7:130523362-130523606 | Common:2; Rare:53 | ||||
chr7:130541040-130541391 | Rare:80 |