Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102714205-102714669 | Common:2; Rare:150 | ||||
chr10:102854155-102854284 | Common:1; Rare:45 | ||||
chr10:103193250-103193450 | Common:4; Rare:62 | ||||
chr10:103351119-103351192 | Common:1; Rare:22 | ||||
chr10:103396411-103396709 | Rare:106 | ||||
chr10:104268912-104269176 | Common:3; Rare:62 | ||||
chr10:109923423-109923661 | Common:2; Rare:91 | ||||
chr10:110304881-110305054 | Common:2; Rare:62 | ||||
chr10:110919322-110919619 | Common:7; Rare:78 | ||||
chr10:112215335-112215535 | Rare:34 | ||||
chr10:112215658-112215787 | Rare:28 | ||||
chr10:112376171-112376249 | Rare:8 | ||||
chr10:112446898-112447295 | Common:3; Rare:98 | ||||
chr10:118754921-118755305 | Common:1; Rare:122 | ||||
chr10:119165631-119165797 | Common:1; Rare:73; Clinvar (benign):4 |