Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75051418-75051655 | Common:3; Rare:66; Clinvar:3; Clinvar (benign):2 | ||||
chr14:75063983-75064184 | Common:1; Rare:50 | ||||
chr14:75069493-75069680 | Common:1; Rare:43 | ||||
chr14:75127001-75127128 | Rare:42 | ||||
chr14:75147737-75148031 | Common:3; Rare:39 | ||||
chr14:75279524-75279660 | Rare:28 | ||||
chr14:75660789-75661334 | Common:4; Rare:132 | ||||
chr14:75661434-75661625 | Common:2; Rare:44 | ||||
chr14:75981125-75981139 | |||||
chr14:76762227-76762340 | Rare:25 | ||||
chr14:76762638-76762974 | Rare:109 | ||||
chr14:76812829-76813035 | Common:2; Rare:76 | ||||
chr14:77028706-77028912 | Rare:70 | ||||
chr14:77097980-77098361 | Rare:124 | ||||
chr14:77141630-77141745 | Common:1; Rare:18 |