Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73058314-73058585 | Common:3; Rare:82 | ||||
chr14:74493570-74493767 | Common:3; Rare:75; Clinvar (benign):3 | ||||
chr14:74713082-74713194 | Rare:56 | ||||
chr14:74881797-74881961 | Common:1; Rare:71 | ||||
chr14:77377082-77377410 | Common:1; Rare:89 | ||||
chr14:77457582-77457852 | Common:1; Rare:81 | ||||
chr14:77708005-77708133 | Common:1; Rare:66 | ||||
chr14:81220871-81221054 | Common:1; Rare:87 | ||||
chr14:88562907-88563079 | Rare:80 | ||||
chr14:92040028-92040187 | Common:2; Rare:43; Clinvar (benign):1 | ||||
chr14:92121673-92121985 | Common:4; Rare:100 | ||||
chr14:93184866-93184961 | Rare:30 | ||||
chr14:93207060-93207284 | Common:2; Rare:113 | ||||
chr14:94081152-94081305 | Common:2; Rare:53 | ||||
chr14:96363318-96363543 | Common:1; Rare:72 |