Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:88824777-88824927 | Rare:45 | ||||
chr14:89350082-89350298 | Rare:45 | ||||
chr14:89954656-89954978 | Rare:98 | ||||
chr14:89955806-89955962 | Common:9; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
chr14:90331894-90332183 | Common:1; Rare:84 | ||||
chr14:90396513-90396576 | Rare:11 | ||||
chr14:90396864-90397237 | Common:5; Rare:175; Clinvar (benign):2 | ||||
chr14:91060122-91060393 | Common:3; Rare:97 | ||||
chr14:91244672-91244822 | Common:2; Rare:27 | ||||
chr14:91510406-91510713 | Common:1; Rare:106 | ||||
chr14:91947030-91947130 | Common:1; Rare:19 | ||||
chr14:92040017-92040159 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
chr14:92121649-92122000 | Common:5; Rare:118 | ||||
chr14:92748594-92748829 | Rare:64 | ||||
chr14:92794024-92794408 | Rare:126 |