Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77457997-77458139 | Rare:38 | ||||
chr14:77616562-77616722 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):3 | ||||
chr14:77707991-77708120 | Rare:61 | ||||
chr14:81220855-81221056 | Common:1; Rare:97 | ||||
chr14:81221242-81221456 | Common:1; Rare:51 | ||||
chr14:85530004-85530184 | Common:1; Rare:38 | ||||
chr14:89954562-89954884 | Common:3; Rare:109 | ||||
chr14:90331918-90332202 | Common:1; Rare:77 | ||||
chr14:90396957-90397226 | Common:5; Rare:125; Clinvar (benign):2 | ||||
chr14:91060565-91060812 | Common:2; Rare:80 | ||||
chr14:91114288-91114402 | Rare:18 | ||||
chr14:91510448-91510644 | Common:1; Rare:63 | ||||
chr14:92040019-92040164 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
chr14:92121667-92121999 | Common:4; Rare:111 | ||||
chr14:92793998-92794408 | Rare:133 |