Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110871718-110871966 | Rare:77 | ||||
chr10:110919326-110919654 | Common:7; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
chr10:112446888-112447273 | Common:3; Rare:94 | ||||
chr10:113854594-113854666 | Rare:18 | ||||
chr10:114821597-114821819 | Common:1; Rare:85 | ||||
chr10:117542605-117542767 | Rare:35 | ||||
chr10:119080630-119080927 | Common:4; Rare:97 | ||||
chr10:119596929-119597151 | Common:1; Rare:59 | ||||
chr10:119892495-119892783 | Common:3; Rare:105 | ||||
chr10:120851167-120851426 | Common:5; Rare:87 | ||||
chr10:121928016-121928068 | Rare:12 | ||||
chr10:122954188-122954458 | Rare:98 | ||||
chr10:123008769-123009026 | Common:6; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791823-124791938 | Rare:55 | ||||
chr10:125823172-125823563 | Common:2; Rare:130; Clinvar:1; Clinvar (benign):2 |