Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110005819-110006098 | Common:4; Rare:70 | ||||
chr10:110007682-110008032 | Rare:104 | ||||
chr10:110567401-110567769 | Common:2; Rare:99; Clinvar:2; Clinvar (benign):5 | ||||
chr10:110871745-110871964 | Rare:65 | ||||
chr10:110919340-110919620 | Common:7; Rare:73 | ||||
chr10:112183708-112183928 | Common:3; Rare:78 | ||||
chr10:112446724-112447293 | Common:3; Rare:138 | ||||
chr10:113679758-113679925 | Common:3; Rare:62 | ||||
chr10:113854352-113854864 | Common:1; Rare:116 | ||||
chr10:114174168-114174311 | Rare:53 | ||||
chr10:118046684-118047008 | Common:4; Rare:105 | ||||
chr10:119080767-119080927 | Rare:63 | ||||
chr10:119178769-119178940 | Common:3; Rare:70 | ||||
chr10:119651210-119651389 | Common:4; Rare:75; Clinvar (benign):2 | ||||
chr10:119892536-119892863 | Common:3; Rare:126 |