Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778591-778819 | Common:5; Rare:97 | ||||
chr1:827520-827667 | Common:1; Rare:58 | ||||
chr1:9687553-9687633 | Common:1; Rare:18 | ||||
chr1:36386541-36386740 | Rare:25 | ||||
chr1:58783132-58783442 | Common:2; Rare:81 | ||||
chr1:67832066-67832224 | Common:1; Rare:37 | ||||
chr1:144551931-144552215 | Rare:92 | ||||
chr1:149636475-149636760 | Common:6; Rare:85 | ||||
chr1:150559094-150559362 | Common:1; Rare:97; Clinvar:3 | ||||
chr1:156130325-156130620 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
chr1:172144602-172144923 | Rare:58 | ||||
chr1:186309656-186309841 | Rare:54 | ||||
chr1:197201253-197201523 | Common:1; Rare:91 | ||||
chr1:222814968-222815078 | Common:3; Rare:43 | ||||
chr1:223992547-223992785 | Common:3; Rare:92 |