Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:72781876-72782183 | Common:1; Rare:116 | ||||
chr13:75549475-75549831 | Common:8; Rare:88 | ||||
chr13:75636023-75636353 | Common:2; Rare:78 | ||||
chr13:75804015-75804215 | Common:1; Rare:33 | ||||
chr13:77027142-77027282 | Common:5; Rare:43 | ||||
chr13:79405795-79405885 | Rare:33 | ||||
chr13:93227139-93227495 | Common:1; Rare:88; Clinvar:6; Clinvar (benign):1 | ||||
chr13:95676930-95677176 | Common:3; Rare:83 | ||||
chr13:96053336-96053536 | Common:2; Rare:93 | ||||
chr13:97222095-97222420 | Rare:58 | ||||
chr13:99200673-99200894 | Common:6; Rare:101 | ||||
chr13:100088849-100089117 | Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596810-102597041 | Common:1; Rare:109 | ||||
chr13:102845734-102846112 | Common:8; Rare:100; Clinvar:3; Clinvar (benign):4 | ||||
chr13:106568069-106568267 | Rare:61 |