Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:120851200-120851411 | Common:4; Rare:73 | ||||
chr10:121927961-121928068 | Rare:35 | ||||
chr10:121928438-121928551 | Rare:29 | ||||
chr10:122954185-122954508 | Common:1; Rare:119 | ||||
chr10:122980329-122980439 | Common:1; Rare:15 | ||||
chr10:123008779-123009028 | Common:5; Rare:68; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791790-124791938 | Common:1; Rare:78 | ||||
chr10:124801687-124801841 | Rare:45 | ||||
chr10:125719427-125719734 | Common:1; Rare:103 | ||||
chr10:125823200-125823568 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896447-125896628 | Common:4; Rare:19 | ||||
chr10:126905275-126905465 | Rare:72 | ||||
chr10:129466984-129467280 | Common:3; Rare:111 | ||||
chr10:130136312-130136459 | Common:6; Rare:61 | ||||
chr10:131981760-131982154 | Common:4; Rare:136 |