Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:103396411-103396709 | Rare:106 | ||||
chr10:103452303-103452442 | Rare:43 | ||||
chr10:103693113-103693377 | Common:1; Rare:70 | ||||
chr10:104121750-104122174 | Common:3; Rare:142 | ||||
chr10:104232308-104232511 | Common:1; Rare:54 | ||||
chr10:104254865-104254935 | Rare:21 | ||||
chr10:104268935-104269208 | Common:3; Rare:66 | ||||
chr10:104353554-104353834 | Common:2; Rare:71 | ||||
chr10:109923423-109923665 | Common:2; Rare:93 | ||||
chr10:109996371-109996395 | Rare:2 | ||||
chr10:110005910-110006127 | Common:3; Rare:66 | ||||
chr10:110007682-110008050 | Common:1; Rare:109 | ||||
chr10:110871614-110871972 | Rare:116 | ||||
chr10:110918923-110918953 | Rare:8 | ||||
chr10:110919124-110919654 | Common:8; Rare:140; Clinvar:1; Clinvar (benign):1 |