Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110567381-110567773 | Common:2; Rare:109; Clinvar:2; Clinvar (benign):5 | ||||
chr10:110568347-110568466 | Common:2; Rare:30 | ||||
chr10:110644060-110644440 | Common:1; Rare:99; Clinvar (benign):1 | ||||
chr10:110823134-110823285 | Rare:26 | ||||
chr10:110871553-110871984 | Rare:130 | ||||
chr10:110872222-110872418 | Rare:63 | ||||
chr10:110918487-110918741 | Common:3; Rare:75 | ||||
chr10:110919199-110919660 | Common:8; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
chr10:110920024-110920456 | Common:3; Rare:167 | ||||
chr10:112183693-112183935 | Common:3; Rare:82 | ||||
chr10:112446825-112447242 | Common:3; Rare:101 | ||||
chr10:112950025-112950365 | Common:3; Rare:74 | ||||
chr10:113679731-113679949 | Common:3; Rare:81 | ||||
chr10:113854099-113854649 | Rare:114 | ||||
chr10:114043683-114043892 | Common:1; Rare:44 |