Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49598849-49599036 | Common:1; Rare:69 | ||||
chr14:49620572-49620820 | Common:2; Rare:99; Clinvar:1 | ||||
chr14:49688160-49688352 | Common:2; Rare:74 | ||||
chr14:49692997-49693170 | Common:1; Rare:58 | ||||
chr14:49768004-49768283 | Common:2; Rare:103 | ||||
chr14:49852741-49853126 | Common:3; Rare:102 | ||||
chr14:49892882-49893112 | Rare:100 | ||||
chr14:50116422-50116705 | Rare:139 | ||||
chr14:50312031-50312396 | Common:3; Rare:154; Clinvar:2; Clinvar (benign):3 | ||||
chr14:50532455-50532761 | Common:4; Rare:95 | ||||
chr14:50561080-50561209 | Rare:24 | ||||
chr14:50668322-50668562 | Common:4; Rare:90 | ||||
chr14:50944378-50944573 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51095051-51095306 | Common:4; Rare:99 | ||||
chr14:51240004-51240436 | Common:2; Rare:150 |