Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110005914-110006106 | Common:3; Rare:59 | ||||
chr10:110007682-110008092 | Common:1; Rare:118 | ||||
chr10:110567391-110567749 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):5 | ||||
chr10:110871745-110871964 | Rare:65 | ||||
chr10:110919133-110919636 | Common:8; Rare:133 | ||||
chr10:112446729-112447284 | Common:3; Rare:133 | ||||
chr10:112950135-112950276 | Common:2; Rare:23 | ||||
chr10:113854386-113854645 | Rare:52 | ||||
chr10:113855035-113855044 | Rare:2 | ||||
chr10:117005153-117005497 | Common:2; Rare:93 | ||||
chr10:117542171-117542788 | Common:3; Rare:158 | ||||
chr10:118045963-118046323 | Common:1; Rare:106 | ||||
chr10:118046454-118046551 | Rare:25 | ||||
chr10:118046667-118047013 | Common:4; Rare:109 | ||||
chr10:118754913-118755271 | Common:1; Rare:119 |