Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12129433-12129719 | Rare:121 | ||||
chr10:12195775-12196248 | Rare:127 | ||||
chr10:13099929-13100302 | Common:4; Rare:89; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13348005-13348280 | Rare:87 | ||||
chr10:13707171-13707382 | Common:3; Rare:38 | ||||
chr10:14838018-14838380 | Common:2; Rare:99 | ||||
chr10:14878637-14878894 | Common:2; Rare:76 | ||||
chr10:14954023-14954195 | Rare:61 | ||||
chr10:15097301-15097401 | Common:1; Rare:50 | ||||
chr10:16436787-16437044 | Common:2; Rare:56 | ||||
chr10:16816987-16817218 | Common:1; Rare:70 | ||||
chr10:16817313-16817744 | Common:5; Rare:153 | ||||
chr10:17201590-17201754 | Common:1; Rare:60 | ||||
chr10:17228603-17228675 | Common:1; Rare:24 | ||||
chr10:17230248-17230454 | Common:1; Rare:45 |