Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113863978-113864177 | Common:2; Rare:54 | ||||
chr13:114132500-114132883 | Common:2; Rare:118 | ||||
chr13:114234971-114235135 | Common:5; Rare:52 | ||||
chr13:114281520-114282018 | Common:8; Rare:277 | ||||
chr13:114286249-114286629 | Rare:110 | ||||
chr14:20333247-20333411 | Common:1; Rare:34 | ||||
chr14:20343407-20343683 | Common:7; Rare:141 | ||||
chr14:20413419-20413521 | Common:2; Rare:29 | ||||
chr14:20450738-20450790 | Rare:15 | ||||
chr14:20454585-20454648 | Rare:22 | ||||
chr14:20454712-20455570 | Common:7; Rare:222 | ||||
chr14:20461321-20461519 | Rare:68 | ||||
chr14:20461716-20462020 | Common:3; Rare:72 | ||||
chr14:20684428-20684630 | Common:2; Rare:32; Clinvar (benign):2 | ||||
chr14:20989737-20990035 | Common:6; Rare:75 |