Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:86755485-86755890 | Common:2; Rare:87 | ||||
chr10:86955570-86955791 | Rare:34 | ||||
chr10:86970229-86970375 | Common:1; Rare:45 | ||||
chr10:86970878-86971099 | Common:3; Rare:45 | ||||
chr10:86971172-86971196 | Rare:5 | ||||
chr10:86971202-86971438 | Common:2; Rare:81 | ||||
chr10:87342254-87342942 | Common:6; Rare:208 | ||||
chr10:87862255-87862570 | Rare:152; Clinvar:1 | ||||
chr10:88939485-88939914 | Common:1; Rare:78; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr10:88942372-88942416 | Rare:10 | ||||
chr10:88948795-88949265 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr10:88953600-88953816 | Rare:44 | ||||
chr10:91807520-91807609 | Rare:21 | ||||
chr10:92240658-92240799 | Rare:31 | ||||
chr10:95393270-95393442 | Common:1; Rare:30 |