Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:90397186-90397233 | Rare:19; Clinvar (benign):2 | ||||
chr14:91060142-91060384 | Common:2; Rare:90 | ||||
chr14:91510251-91510715 | Common:1; Rare:161 | ||||
chr14:91836404-91836688 | Common:12; Rare:50 | ||||
chr14:91946971-91947108 | Common:1; Rare:18 | ||||
chr14:92039756-92039913 | Rare:31; Clinvar:1 | ||||
chr14:92040011-92040188 | Common:3; Rare:56; Clinvar:3; Clinvar (benign):2 | ||||
chr14:92121647-92122002 | Common:5; Rare:120 | ||||
chr14:92748510-92748794 | Rare:69 | ||||
chr14:92793967-92794265 | Rare:85 | ||||
chr14:93115144-93115459 | Common:1; Rare:119 | ||||
chr14:93184845-93185017 | Rare:58 | ||||
chr14:93206972-93207317 | Common:3; Rare:172 | ||||
chr14:93332473-93332676 | Common:1; Rare:61 | ||||
chr14:94051352-94051565 | Rare:61 |