Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77320818-77321087 | Rare:85; Clinvar:3 | ||||
chr14:77377055-77377412 | Common:2; Rare:102 | ||||
chr14:77457550-77457884 | Common:1; Rare:98 | ||||
chr14:77708000-77708133 | Common:1; Rare:68 | ||||
chr14:81220871-81221163 | Common:1; Rare:134 | ||||
chr14:88562933-88563075 | Rare:67 | ||||
chr14:89619130-89619282 | Rare:59 | ||||
chr14:90396870-90397162 | Common:5; Rare:145 | ||||
chr14:91510285-91510624 | Common:1; Rare:103 | ||||
chr14:92040019-92040132 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
chr14:92121658-92122000 | Common:4; Rare:115 | ||||
chr14:92793995-92794408 | Rare:135 | ||||
chr14:93184878-93185004 | Rare:39 | ||||
chr14:93207011-93207288 | Common:2; Rare:136 | ||||
chr14:94081150-94081333 | Common:3; Rare:61 |