Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23692516-23692859 | Common:5; Rare:64 | ||||
chr14:24036326-24036451 | Common:3; Rare:49 | ||||
chr14:31109585-31109742 | Common:1; Rare:27 | ||||
chr14:32203267-32203616 | Common:13; Rare:146 | ||||
chr14:34874090-34874206 | Common:1; Rare:31 | ||||
chr14:35336480-35336761 | Common:2; Rare:74 | ||||
chr14:41605293-41605396 | Common:2; Rare:22 | ||||
chr14:49633938-49634043 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49789563-49789659 | Rare:21 | ||||
chr14:49862639-49863050 | Common:1; Rare:186 | ||||
chr14:61718693-61718874 | Rare:42 | ||||
chr14:61751064-61751223 | Rare:41 | ||||
chr14:64186230-64186578 | Common:1; Rare:107; Clinvar:4; Clinvar (benign):1 | ||||
chr14:69049779-69049953 | Rare:38 | ||||
chr14:73785936-73786033 | Rare:19 |