Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:34435263-34435577 | Common:4; Rare:65 | ||||
chr14:34568672-34568847 | Rare:45 | ||||
chr14:35004286-35004351 | Rare:11 | ||||
chr14:35307764-35308088 | Rare:58 | ||||
chr14:35314361-35314531 | Common:2; Rare:32 | ||||
chr14:39037218-39037465 | Common:2; Rare:40 | ||||
chr14:39048396-39048706 | Common:3; Rare:75 | ||||
chr14:39069355-39069405 | Rare:10 | ||||
chr14:44982631-44982854 | Common:1; Rare:32 | ||||
chr14:45108167-45108523 | Rare:68 | ||||
chr14:45873318-45873359 | Rare:7 | ||||
chr14:49621753-49621982 | Rare:67; Clinvar:1; Clinvar (benign):1 | ||||
chr14:49622061-49622311 | Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
chr14:49622374-49622573 | Rare:46; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:49622703-49623076 | Common:1; Rare:76; Clinvar:2 |