Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49598633-49599014 | Common:3; Rare:148 | ||||
chr14:49620573-49620840 | Common:2; Rare:111; Clinvar:3 | ||||
chr14:49892940-49893168 | Rare:93 | ||||
chr14:50312193-50312375 | Rare:71 | ||||
chr14:50532460-50532739 | Common:3; Rare:84 | ||||
chr14:50668295-50668556 | Common:3; Rare:95 | ||||
chr14:50944191-50944662 | Common:8; Rare:160; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr14:51651649-51651958 | Common:4; Rare:89 | ||||
chr14:52552520-52552836 | Common:1; Rare:91 | ||||
chr14:52791591-52791856 | Common:2; Rare:97 | ||||
chr14:55027049-55027399 | Common:4; Rare:88 | ||||
chr14:55191512-55191746 | Common:5; Rare:53 | ||||
chr14:55580080-55580259 | Common:1; Rare:73 | ||||
chr14:57268653-57269094 | Common:2; Rare:140 | ||||
chr14:58298113-58298442 | Rare:80 |