Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6587831-6588136 | Rare:89 | ||||
chr1:8862888-8863063 | Rare:40 | ||||
chr1:9182263-9182471 | Common:2; Rare:58 | ||||
chr1:9244770-9244953 | Common:2; Rare:44; Clinvar (benign):1 | ||||
chr1:9629821-9630017 | Common:2; Rare:49 | ||||
chr1:9687517-9687647 | Common:1; Rare:35 | ||||
chr1:9714474-9714634 | Rare:28 | ||||
chr1:9723045-9723239 | Rare:41; Clinvar (benign):1 | ||||
chr1:9731284-9731492 | Common:4; Rare:62 | ||||
chr1:10149009-10149248 | Common:1; Rare:36 | ||||
chr1:11087863-11088157 | Common:3; Rare:82 | ||||
chr1:11729673-11729792 | Common:4; Rare:24 | ||||
chr1:12150531-12150729 | Common:3; Rare:40 | ||||
chr1:12153304-12153554 | Common:4; Rare:42 | ||||
chr1:12173788-12173826 | Rare:7 |