Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7954173-7954293 | Rare:30 | ||||
chr1:7961442-7961792 | Common:4; Rare:122; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8026289-8026500 | Common:2; Rare:95 | ||||
chr1:8878578-8878833 | Rare:130 | ||||
chr1:9942783-9942912 | Common:1; Rare:21 | ||||
chr1:9942938-9943133 | Common:2; Rare:52 | ||||
chr1:9943291-9943513 | Common:2; Rare:61 | ||||
chr1:10032714-10032965 | Rare:71 | ||||
chr1:10033479-10033673 | Rare:36 | ||||
chr1:10398833-10399125 | Common:2; Rare:115 | ||||
chr1:11099791-11099921 | Common:1; Rare:56 | ||||
chr1:11262511-11262817 | Common:1; Rare:90 | ||||
chr1:11805922-11806256 | Common:2; Rare:87; Clinvar:1 | ||||
chr1:11934553-11934754 | Common:3; Rare:66; Clinvar:5; Clinvar (benign):1 | ||||
chr1:12618180-12618318 | Common:2; Rare:34 |