Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:89954656-89954950 | Rare:90 | ||||
chr14:90396870-90397172 | Common:5; Rare:149 | ||||
chr14:90397175-90397232 | Rare:20; Clinvar (benign):2 | ||||
chr14:91114257-91114402 | Rare:29 | ||||
chr14:91510239-91510624 | Common:1; Rare:123 | ||||
chr14:91836445-91836688 | Common:12; Rare:45 | ||||
chr14:91947011-91947136 | Common:1; Rare:21 | ||||
chr14:92039766-92039777 | Rare:2 | ||||
chr14:92040008-92040132 | Common:3; Rare:42; Clinvar:3; Clinvar (benign):2 | ||||
chr14:92121643-92122005 | Common:5; Rare:126 | ||||
chr14:92748501-92748819 | Rare:78 | ||||
chr14:93184837-93185005 | Rare:56 | ||||
chr14:93206994-93207298 | Common:2; Rare:150 | ||||
chr14:93976524-93976860 | Rare:66 | ||||
chr14:94081120-94081387 | Common:5; Rare:83 |