Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:238203591-238203815 | Common:3; Rare:97 | ||||
chr2:239401645-239401764 | Rare:58 | ||||
chr2:240025297-240025413 | Rare:47; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:240560766-240560873 | Common:1; Rare:46 | ||||
chr2:240682833-240683123 | Rare:51 | ||||
chr2:241102278-241102506 | Common:2; Rare:67 | ||||
chr2:241271929-241271997 | Rare:15 | ||||
chr2:241272770-241272984 | Rare:77 | ||||
chr2:241315109-241315285 | Common:1; Rare:66 | ||||
chr2:241315647-241315989 | Common:5; Rare:133 | ||||
chr2:241508530-241508872 | Common:2; Rare:108 | ||||
chr2:241637544-241637710 | Common:1; Rare:91 | ||||
chr2:241686784-241687029 | Common:2; Rare:70 | ||||
chr2:241701897-241702080 | Rare:73 | ||||
chr2:241734479-241734635 | Common:5; Rare:59 |