Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156127359-156127471 | Common:1; Rare:14 | ||||
chr1:156130196-156130629 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
chr1:156214353-156214478 | Common:1; Rare:16 | ||||
chr1:156281880-156282008 | Common:2; Rare:22 | ||||
chr1:156445919-156446120 | Rare:38 | ||||
chr1:156456490-156457042 | Common:3; Rare:113 | ||||
chr1:156457185-156457588 | Common:1; Rare:77 | ||||
chr1:156457680-156457767 | Rare:17 | ||||
chr1:156463946-156464143 | Rare:48 | ||||
chr1:156465163-156465207 | Rare:11 | ||||
chr1:156501792-156501923 | Common:1; Rare:25 | ||||
chr1:156502920-156503166 | Common:1; Rare:46 | ||||
chr1:156503266-156503657 | Common:2; Rare:72 | ||||
chr1:156504994-156505298 | Common:4; Rare:66 | ||||
chr1:156505347-156505608 | Common:2; Rare:77 |