Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:91510251-91510601 | Common:1; Rare:110 | ||||
chr14:92040023-92040181 | Common:2; Rare:47; Clinvar (benign):1 | ||||
chr14:92121658-92121990 | Common:4; Rare:109 | ||||
chr14:92794004-92794375 | Rare:113 | ||||
chr14:92923066-92923150 | Common:2; Rare:21 | ||||
chr14:93184851-93185004 | Rare:49 | ||||
chr14:93207038-93207285 | Common:2; Rare:123 | ||||
chr14:93430616-93431000 | Rare:69 | ||||
chr14:94081133-94081313 | Common:3; Rare:62 | ||||
chr14:95157424-95157685 | Common:4; Rare:93 | ||||
chr14:95534582-95534694 | Rare:43 | ||||
chr14:96363314-96363552 | Common:1; Rare:80 | ||||
chr14:96502286-96502586 | Common:1; Rare:128 | ||||
chr14:100238532-100238848 | Common:3; Rare:90 | ||||
chr14:100376273-100376514 | Common:3; Rare:78 |