Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:70416973-70417140 | Rare:51 | ||||
chr14:73058249-73058595 | Common:3; Rare:113 | ||||
chr14:73458513-73458849 | Common:5; Rare:86 | ||||
chr14:73567951-73568129 | Rare:49 | ||||
chr14:73644901-73645034 | Common:2; Rare:36; Clinvar:2 | ||||
chr14:73714353-73714488 | Common:1; Rare:46 | ||||
chr14:73886735-73886893 | Common:2; Rare:56 | ||||
chr14:73950050-73950322 | Common:6; Rare:114; Clinvar (benign):5 | ||||
chr14:74019262-74019455 | Common:1; Rare:70 | ||||
chr14:74084397-74084646 | Common:3; Rare:64 | ||||
chr14:74493277-74493781 | Common:4; Rare:157; Clinvar:2; Clinvar (benign):4 | ||||
chr14:74713042-74713198 | Rare:89 | ||||
chr14:74763132-74763397 | Rare:81 | ||||
chr14:75002710-75002947 | Common:1; Rare:73; Clinvar:2 | ||||
chr14:75127001-75127110 | Rare:33 |