Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156337814-156338066 | Rare:53 | ||||
chr1:156338149-156338653 | Common:4; Rare:174 | ||||
chr1:156338676-156338911 | Rare:64 | ||||
chr1:156499857-156500523 | Common:3; Rare:173 | ||||
chr1:156500527-156500596 | Rare:21 | ||||
chr1:156500686-156501298 | Common:3; Rare:211 | ||||
chr1:156501324-156501564 | Rare:67 | ||||
chr1:156572228-156572293 | Rare:8 | ||||
chr1:156572468-156572666 | Common:2; Rare:71 | ||||
chr1:156591556-156591891 | Common:6; Rare:133 | ||||
chr1:156591952-156592246 | Common:1; Rare:93; Clinvar (pathogenic):2 | ||||
chr1:156592348-156592434 | Common:1; Rare:27; Clinvar:1 | ||||
chr1:156592743-156593013 | Common:2; Rare:44 | ||||
chr1:156600880-156600981 | Common:1; Rare:16 | ||||
chr1:156600993-156601075 | Common:1; Rare:17 |