Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:64222964-64223227 | Common:1; Rare:74; Clinvar:4; Clinvar (benign):2 | ||||
chr14:68547633-68547803 | Common:1; Rare:19 | ||||
chr14:68632310-68632499 | Rare:34 | ||||
chr14:69682877-69683141 | Common:3; Rare:44 | ||||
chr14:75258726-75258826 | Rare:18 | ||||
chr14:75258858-75259398 | Common:2; Rare:132 | ||||
chr14:75274976-75275144 | Common:1; Rare:22 | ||||
chr14:75277024-75277327 | Common:1; Rare:66 | ||||
chr14:75277475-75277599 | Rare:32 | ||||
chr14:75294032-75294502 | Common:3; Rare:116 | ||||
chr14:75310751-75311006 | Rare:65 | ||||
chr14:75426679-75426963 | Rare:47 | ||||
chr14:75523877-75524020 | Common:1; Rare:23 | ||||
chr14:75595937-75596204 | Rare:59 | ||||
chr14:75981818-75982047 | Common:2; Rare:52 |