Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:32203220-32203583 | Common:13; Rare:166 | ||||
chr14:34873893-34874206 | Common:3; Rare:62 | ||||
chr14:40954362-40954782 | Common:5; Rare:157 | ||||
chr14:44962738-44962943 | Rare:48 | ||||
chr14:47794998-47795180 | Common:2; Rare:68 | ||||
chr14:47901640-47901923 | Common:2; Rare:81 | ||||
chr14:49633917-49634053 | Common:1; Rare:59; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49789296-49789505 | Rare:51 | ||||
chr14:49861795-49861994 | Rare:46 | ||||
chr14:49862651-49863050 | Common:1; Rare:182 | ||||
chr14:52001506-52001857 | Common:1; Rare:71 | ||||
chr14:54569514-54569659 | Rare:27 | ||||
chr14:57112655-57112730 | Rare:20 | ||||
chr14:58533504-58533666 | Common:1; Rare:29 | ||||
chr14:58639968-58640168 | Common:1; Rare:36 |