Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:104338379-104338528 | Rare:40 | ||||
chr10:110007637-110008016 | Rare:123 | ||||
chr10:110567391-110567749 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):5 | ||||
chr10:110871655-110871964 | Rare:99 | ||||
chr10:110919134-110919636 | Common:8; Rare:133 | ||||
chr10:112183739-112183842 | Common:2; Rare:42 | ||||
chr10:112446839-112447284 | Common:3; Rare:113 | ||||
chr10:113679369-113679629 | Common:1; Rare:54 | ||||
chr10:113854204-113854243 | Rare:10 | ||||
chr10:113854352-113854885 | Common:1; Rare:121 | ||||
chr10:118046678-118047022 | Common:4; Rare:109 | ||||
chr10:118754913-118755288 | Common:1; Rare:125 | ||||
chr10:119080772-119080923 | Rare:59 | ||||
chr10:119165648-119165803 | Rare:70; Clinvar (benign):3 | ||||
chr10:119178786-119178935 | Common:3; Rare:59 |