Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:219635535-219635747 | Common:3; Rare:58 | ||||
chr2:219685033-219685327 | Common:1; Rare:81 | ||||
chr2:226631721-226631898 | Rare:35 | ||||
chr2:226755151-226755440 | Common:2; Rare:43 | ||||
chr2:226796111-226796242 | Rare:52 | ||||
chr2:226798766-226798798 | Rare:8 | ||||
chr2:226801140-226801318 | Rare:58 | ||||
chr2:231401041-231401384 | Common:5; Rare:97 | ||||
chr2:231403732-231403988 | Common:2; Rare:48 | ||||
chr2:231514317-231514577 | Common:5; Rare:105 | ||||
chr2:231604627-231604931 | Common:21; Rare:110 | ||||
chr2:237360108-237360268 | Rare:36; Clinvar:4; Clinvar (benign):3 | ||||
chr2:240256038-240256210 | Rare:42 | ||||
chr2:241253022-241253048 | Rare:8 | ||||
chr2:241881275-241881396 | Rare:29 |