Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74493395-74493770 | Common:4; Rare:120; Clinvar (benign):4 | ||||
chr14:74713058-74713200 | Rare:79 | ||||
chr14:74881827-74881982 | Rare:72 | ||||
chr14:75127033-75127106 | Rare:17 | ||||
chr14:75660792-75660962 | Rare:44 | ||||
chr14:75661168-75661320 | Common:2; Rare:42 | ||||
chr14:75981125-75981304 | Rare:31 | ||||
chr14:77377052-77377410 | Common:2; Rare:105 | ||||
chr14:77457550-77457781 | Common:1; Rare:76 | ||||
chr14:77708000-77708131 | Common:1; Rare:66 | ||||
chr14:81220867-81221046 | Common:1; Rare:86 | ||||
chr14:81221288-81221471 | Common:1; Rare:46 | ||||
chr14:81436398-81436625 | Common:4; Rare:86 | ||||
chr14:85530030-85530184 | Common:1; Rare:34 | ||||
chr14:90396870-90397102 | Common:2; Rare:121 |