Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:89301869-89302095 | Rare:49 | ||||
chr10:89327942-89328036 | Common:1; Rare:14 | ||||
chr10:89414676-89414800 | Common:3; Rare:63 | ||||
chr10:89643801-89644181 | Rare:77 | ||||
chr10:89701391-89701617 | Common:2; Rare:69 | ||||
chr10:91633052-91633253 | Common:2; Rare:61 | ||||
chr10:91798290-91798386 | Rare:31 | ||||
chr10:92290998-92291384 | Common:5; Rare:123 | ||||
chr10:92573947-92574129 | Common:1; Rare:62 | ||||
chr10:92592952-92593169 | Common:3; Rare:63 | ||||
chr10:93482277-93482322 | Rare:7 | ||||
chr10:93600390-93600833 | Common:3; Rare:119; Clinvar (pathogenic):1 | ||||
chr10:93601172-93601478 | Common:3; Rare:66 | ||||
chr10:94683381-94683591 | Common:1; Rare:45 | ||||
chr10:94683713-94683987 | Common:1; Rare:72 |