Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:97633709-97633832 | Common:2; Rare:39 | ||||
chr9:98192605-98192883 | Common:6; Rare:76 | ||||
chr9:98255587-98255843 | Common:3; Rare:79 | ||||
chr9:99221915-99222357 | Common:2; Rare:172; Clinvar:2; Clinvar (benign):2 | ||||
chr9:99906570-99906697 | Rare:64 | ||||
chr9:100098959-100099314 | Common:3; Rare:100; Clinvar:2 | ||||
chr9:100352831-100353081 | Rare:90 | ||||
chr9:101398521-101398910 | Common:1; Rare:140 | ||||
chr9:101487040-101487140 | Rare:31 | ||||
chr9:101533587-101533899 | Common:2; Rare:88 | ||||
chr9:107488133-107488588 | Common:3; Rare:145 | ||||
chr9:107489767-107490061 | Common:4; Rare:127 | ||||
chr9:108934055-108934477 | Common:7; Rare:166; Clinvar:2; Clinvar (benign):2 | ||||
chr9:109497877-109497995 | Common:1; Rare:36 | ||||
chr9:109498227-109498485 | Common:1; Rare:78 |