Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25247419-25247691 | Common:4; Rare:104 | ||||
chr1:25338214-25338447 | Common:1; Rare:80 | ||||
chr1:25430735-25431101 | Common:2; Rare:129 | ||||
chr1:25819892-25820219 | Common:4; Rare:97 | ||||
chr1:25859370-25859556 | Common:2; Rare:76 | ||||
chr1:25906392-25906538 | Rare:57 | ||||
chr1:26279934-26280182 | Rare:137 | ||||
chr1:26432099-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472270-26472532 | Common:4; Rare:85 | ||||
chr1:26787870-26787987 | Common:1; Rare:41; Clinvar (benign):1 | ||||
chr1:26900438-26900547 | Rare:37 | ||||
chr1:26921507-26921815 | Common:3; Rare:90 | ||||
chr1:27321983-27322336 | Common:1; Rare:128 | ||||
chr1:27725693-27725994 | Common:2; Rare:86 | ||||
chr1:27772920-27773325 | Common:1; Rare:130 |