Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100996940-100997165 | Common:2; Rare:63 | ||||
chr10:100998105-100998392 | Common:1; Rare:68 | ||||
chr10:100998645-100998692 | Rare:5 | ||||
chr10:100999654-100999924 | Common:2; Rare:84 | ||||
chr10:101031102-101031286 | Common:1; Rare:43 | ||||
chr10:101588120-101588348 | Rare:99; Clinvar:1 | ||||
chr10:101694859-101695154 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr10:101818088-101818208 | Rare:40 | ||||
chr10:101818323-101818803 | Common:1; Rare:128 | ||||
chr10:101839803-101839908 | Rare:36 | ||||
chr10:102056106-102056359 | Common:1; Rare:61 | ||||
chr10:102114937-102115128 | Common:2; Rare:55 | ||||
chr10:102120456-102120760 | Common:1; Rare:101 | ||||
chr10:102152028-102152423 | Common:3; Rare:123 | ||||
chr10:102395609-102395735 | Rare:34 |