Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:30546645-30546727 | Rare:17 | ||||
chr14:37564185-37564272 | Rare:12 | ||||
chr14:37584819-37585053 | Common:3; Rare:54 | ||||
chr14:49633909-49634043 | Common:1; Rare:60; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49862639-49862872 | Common:1; Rare:121 | ||||
chr14:66486295-66486371 | Rare:14 | ||||
chr14:67620687-67620944 | Common:1; Rare:52 | ||||
chr14:73590107-73590272 | Common:2; Rare:36 | ||||
chr14:74067480-74067640 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
chr14:74567876-74568109 | Common:3; Rare:44 | ||||
chr14:75981817-75982092 | Common:2; Rare:67 | ||||
chr14:77026041-77026376 | Rare:115 | ||||
chr14:81170384-81170484 | Rare:27 | ||||
chr14:92934588-92934842 | Common:3; Rare:58 | ||||
chr14:95516614-95516778 | Common:2; Rare:39 |