Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89009106-89009396 | Common:1; Rare:58 | ||||
chr1:89009406-89009611 | Common:3; Rare:52 | ||||
chr1:89108271-89108472 | Common:2; Rare:45 | ||||
chr1:89110165-89110363 | Rare:44 | ||||
chr1:89127418-89127593 | Rare:49 | ||||
chr1:91511374-91511668 | Rare:57 | ||||
chr1:91817578-91817933 | Common:2; Rare:40 | ||||
chr1:91851312-91851517 | Rare:40 | ||||
chr1:92833469-92833675 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr1:92837174-92837633 | Common:1; Rare:120; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:94247604-94247839 | Common:2; Rare:66 | ||||
chr1:100038832-100038863 | Rare:9 | ||||
chr1:100628943-100629088 | Common:1; Rare:18 | ||||
chr1:100724336-100724890 | Common:2; Rare:120 | ||||
chr1:107786681-107786791 | Common:1; Rare:18 |