Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:39170268-39170472 | Common:3; Rare:64 | ||||
chr14:39174970-39175321 | Common:5; Rare:124 | ||||
chr14:39267057-39267422 | Common:2; Rare:129 | ||||
chr14:39432418-39432657 | Common:6; Rare:81 | ||||
chr14:44961892-44962272 | Common:3; Rare:110 | ||||
chr14:45083904-45084174 | Common:2; Rare:102 | ||||
chr14:45135723-45135979 | Common:1; Rare:48 | ||||
chr14:45253065-45253426 | Common:1; Rare:106 | ||||
chr14:49586335-49586753 | Common:1; Rare:224 | ||||
chr14:49598719-49599014 | Common:2; Rare:109 | ||||
chr14:49620561-49620812 | Common:2; Rare:100 | ||||
chr14:49795900-49796180 | Rare:44 | ||||
chr14:49892898-49893154 | Rare:109 | ||||
chr14:50116557-50116641 | Rare:45 | ||||
chr14:50312125-50312374 | Rare:107; Clinvar:1; Clinvar (benign):1 |