Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4540020-4540216 | Rare:49 | ||||
chr19:4723755-4724075 | Common:7; Rare:126 | ||||
chr19:4831647-4831834 | Common:3; Rare:48 | ||||
chr19:4867626-4867901 | Common:4; Rare:79 | ||||
chr19:5293211-5293421 | Common:1; Rare:94 | ||||
chr19:5622701-5623317 | Common:6; Rare:243 | ||||
chr19:5680924-5681034 | Rare:29 | ||||
chr19:5775080-5775175 | Rare:21 | ||||
chr19:5978062-5978393 | Common:3; Rare:124 | ||||
chr19:6110416-6110821 | Common:2; Rare:120 | ||||
chr19:6381123-6381383 | Common:3; Rare:103 | ||||
chr19:6393371-6393591 | Common:2; Rare:65 | ||||
chr19:6693410-6693724 | Common:5; Rare:83; Clinvar (benign):1 | ||||
chr19:6720516-6720805 | Common:2; Rare:70; Clinvar (benign):2 | ||||
chr19:6730553-6730757 | Common:4; Rare:36 |