Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619643-112619842 | Common:1; Rare:69 | ||||
chr1:117929600-117929771 | Rare:50 | ||||
chr1:145823922-145824241 | Rare:111 | ||||
chr1:145927437-145927566 | Common:1; Rare:36; Clinvar (pathogenic):1 | ||||
chr1:145964421-145964742 | Rare:70 | ||||
chr1:147172427-147172710 | Common:1; Rare:69 | ||||
chr1:149886674-149886923 | Rare:73 | ||||
chr1:149887944-149888213 | Rare:63 | ||||
chr1:151165840-151166157 | Common:3; Rare:86 | ||||
chr1:154220545-154220961 | Common:1; Rare:141 | ||||
chr1:154974374-154974712 | Rare:82 | ||||
chr1:155859362-155859567 | Common:1; Rare:47 | ||||
chr1:156114539-156114711 | Rare:33; Clinvar:1 | ||||
chr1:156212981-156213007 | Rare:4 | ||||
chr1:156338197-156338542 | Common:2; Rare:125 |