Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659264-99659531 | Common:1; Rare:66 | ||||
chr10:99732067-99732314 | Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
chr10:100987433-100987595 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr10:101031126-101031488 | Common:1; Rare:83 | ||||
chr10:101588157-101588327 | Rare:72 | ||||
chr10:102714267-102714669 | Common:2; Rare:131 | ||||
chr10:103396442-103396727 | Rare:101 | ||||
chr10:103917625-103917897 | Rare:56 | ||||
chr10:104338409-104338528 | Rare:33 | ||||
chr10:110006021-110006084 | Rare:14 | ||||
chr10:110007682-110008013 | Rare:100 | ||||
chr10:110919355-110919645 | Common:7; Rare:79; Clinvar:1 | ||||
chr10:112446904-112447246 | Common:3; Rare:81 | ||||
chr10:113854600-113854666 | Rare:17 | ||||
chr10:114821655-114821780 | Common:1; Rare:50 |