Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235128735-235129108 | Common:1; Rare:151 | ||||
chr1:235327913-235328104 | Rare:53 | ||||
chr1:235328109-235328537 | Common:3; Rare:121 | ||||
chr1:235328788-235329018 | Common:1; Rare:76 | ||||
chr1:235504397-235504762 | Common:4; Rare:116 | ||||
chr1:239719100-239719259 | Common:1; Rare:28 | ||||
chr1:243255326-243255433 | Rare:28 | ||||
chr1:243255729-243256188 | Common:1; Rare:137; Clinvar:5; Clinvar (benign):1 | ||||
chr1:244048239-244048543 | Rare:95 | ||||
chr1:244051165-244051304 | Rare:9 | ||||
chr1:244461347-244461558 | Rare:75 | ||||
chr1:244835185-244835341 | Rare:64 | ||||
chr1:244835375-244835755 | Common:4; Rare:156; Clinvar (benign):5 | ||||
chr1:244856486-244856743 | Common:1; Rare:64; Clinvar (benign):2 | ||||
chr1:244863646-244864206 | Common:1; Rare:191; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 |