Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110007661-110008092 | Common:1; Rare:125 | ||||
chr10:110076975-110077075 | Rare:20 | ||||
chr10:110225895-110226249 | Common:2; Rare:98 | ||||
chr10:110227235-110227406 | Common:2; Rare:22 | ||||
chr10:110644181-110644457 | Common:1; Rare:74; Clinvar (benign):3 | ||||
chr10:110871737-110871964 | Rare:70 | ||||
chr10:110919134-110919636 | Common:8; Rare:133 | ||||
chr10:112446729-112447294 | Common:3; Rare:137 | ||||
chr10:113663801-113664314 | Common:2; Rare:107 | ||||
chr10:113854182-113854983 | Common:2; Rare:183 | ||||
chr10:114821647-114821985 | Common:1; Rare:110 | ||||
chr10:117374770-117374969 | Common:1; Rare:66 | ||||
chr10:118046581-118047013 | Common:4; Rare:136 | ||||
chr10:118754925-118755315 | Common:1; Rare:129 | ||||
chr10:119080748-119080923 | Rare:65 |