Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49633956-49634084 | Common:1; Rare:54; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49774435-49774633 | Common:2; Rare:47 | ||||
chr14:49799476-49799660 | Rare:59 | ||||
chr14:49834436-49834459 | Rare:6 | ||||
chr14:49862861-49863071 | Rare:70 | ||||
chr14:50000247-50000292 | Common:1; Rare:8 | ||||
chr14:50528155-50528240 | Rare:11 | ||||
chr14:51396247-51396628 | Common:2; Rare:82 | ||||
chr14:51652724-51652777 | Rare:8 | ||||
chr14:51653011-51653482 | Common:3; Rare:80 | ||||
chr14:51656854-51656904 | Rare:11 | ||||
chr14:51658127-51658309 | Common:2; Rare:32 | ||||
chr14:51659969-51660617 | Common:6; Rare:93 | ||||
chr14:51660652-51661099 | Common:1; Rare:98 | ||||
chr14:51669438-51669578 | Common:1; Rare:24 |