Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:114296482-114296648 | Rare:40 | ||||
chr14:21069374-21069676 | Common:1; Rare:64 | ||||
chr14:22845554-22845898 | Rare:91 | ||||
chr14:31109514-31109734 | Common:2; Rare:52 | ||||
chr14:32203267-32203583 | Common:13; Rare:134 | ||||
chr14:34764869-34765109 | Rare:65 | ||||
chr14:39526437-39526617 | Rare:71 | ||||
chr14:49633936-49634070 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49789529-49789756 | Rare:50 | ||||
chr14:49862631-49863036 | Common:1; Rare:183 | ||||
chr14:64222964-64223273 | Common:1; Rare:88; Clinvar:5; Clinvar (benign):3 | ||||
chr14:64224812-64225040 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
chr14:65468382-65468498 | Common:1; Rare:16 | ||||
chr14:68560057-68560332 | Rare:46 | ||||
chr14:68795244-68795425 | Common:3; Rare:40 |