Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:109923400-109923641 | Common:2; Rare:85 | ||||
chr10:110567355-110567749 | Common:3; Rare:110; Clinvar:1; Clinvar (benign):5 | ||||
chr10:110871652-110871941 | Rare:89 | ||||
chr10:110919298-110919629 | Common:7; Rare:85 | ||||
chr10:112376160-112376286 | Rare:19 | ||||
chr10:112446893-112447285 | Common:3; Rare:98 | ||||
chr10:119892548-119892772 | Common:3; Rare:85 | ||||
chr10:125719462-125719734 | Common:1; Rare:86 | ||||
chr10:125823192-125823552 | Common:1; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896300-125896585 | Common:2; Rare:15 | ||||
chr10:126905302-126905458 | Rare:60 | ||||
chr10:129466953-129467273 | Common:4; Rare:130 | ||||
chr10:133276859-133277040 | Rare:46 | ||||
chr10:133308835-133309094 | Common:2; Rare:104 | ||||
chr11:207381-207516 | Common:4; Rare:50 |