Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49598672-49598976 | Common:1; Rare:120 | ||||
chr14:49620563-49620835 | Common:2; Rare:113; Clinvar:3 | ||||
chr14:49892912-49893136 | Rare:92 | ||||
chr14:50312152-50312376 | Rare:98 | ||||
chr14:50532503-50532773 | Common:3; Rare:88 | ||||
chr14:50668322-50668556 | Common:3; Rare:86 | ||||
chr14:50944399-50944590 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51651691-51651984 | Common:4; Rare:84 | ||||
chr14:52004158-52004238 | Common:1; Rare:33 | ||||
chr14:52069000-52069215 | Common:2; Rare:49 | ||||
chr14:52314224-52314319 | Rare:33 | ||||
chr14:52707045-52707298 | Common:1; Rare:104 | ||||
chr14:52791457-52791757 | Common:1; Rare:105 | ||||
chr14:52951003-52951442 | Common:4; Rare:157 | ||||
chr14:53953385-53953639 | Common:2; Rare:72 |