Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110210014-110210315 | Common:1; Rare:58 | ||||
chr10:110225791-110226281 | Common:2; Rare:136 | ||||
chr10:110567391-110567804 | Common:2; Rare:124; Clinvar:2; Clinvar (benign):5 | ||||
chr10:110871622-110871976 | Rare:117 | ||||
chr10:110918923-110918988 | Rare:18 | ||||
chr10:110919134-110919636 | Common:8; Rare:133 | ||||
chr10:112183684-112183879 | Common:3; Rare:72 | ||||
chr10:112446853-112447294 | Common:3; Rare:113 | ||||
chr10:112949938-112950329 | Common:3; Rare:85 | ||||
chr10:112951004-112951256 | Common:2; Rare:65 | ||||
chr10:113678889-113679200 | Common:4; Rare:45 | ||||
chr10:113679803-113679938 | Common:2; Rare:53 | ||||
chr10:113854352-113854869 | Common:1; Rare:118 | ||||
chr10:114174160-114174244 | Rare:39 | ||||
chr10:114526806-114527193 | Common:4; Rare:74 |