Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:166999074-166999397 | Common:1; Rare:109 | ||||
chr6:169701955-169702349 | Common:5; Rare:167 | ||||
chr6:169751574-169751658 | Rare:38; Clinvar (benign):2 | ||||
chr6:170306576-170306812 | Common:1; Rare:75 | ||||
chr6:170553235-170553340 | Common:1; Rare:49 | ||||
chr6:170554184-170554420 | Common:1; Rare:70 | ||||
chr6:170584605-170584776 | Common:1; Rare:51 | ||||
chr7:727230-727314 | Rare:30; Clinvar:1 | ||||
chr7:1504318-1504414 | Common:1; Rare:51 | ||||
chr7:1537260-1537483 | Rare:74 | ||||
chr7:1570004-1570110 | Common:1; Rare:31 | ||||
chr7:2232882-2233210 | Common:1; Rare:109 | ||||
chr7:2242173-2242270 | Common:2; Rare:57 | ||||
chr7:2354045-2354095 | Rare:27 | ||||
chr7:2354542-2354933 | Common:5; Rare:164 |