Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19287935-19288077 | Rare:27 | ||||
chr1:20153980-20154148 | Common:2; Rare:22 | ||||
chr1:20604817-20604952 | Common:1; Rare:27 | ||||
chr1:20654345-20654633 | Common:4; Rare:86; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:21550265-21550361 | Rare:14 | ||||
chr1:22025181-22025522 | Common:7; Rare:84 | ||||
chr1:23082323-23082509 | Rare:39 | ||||
chr1:23397543-23397895 | Common:1; Rare:110 | ||||
chr1:23854504-23854682 | Rare:43; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:24321895-24321997 | Common:1; Rare:22 | ||||
chr1:24839596-24839914 | Rare:63 | ||||
chr1:26225367-26225641 | Common:1; Rare:53 | ||||
chr1:26457634-26457827 | Common:2; Rare:37 | ||||
chr1:27369441-27369667 | Common:1; Rare:47 | ||||
chr1:28581869-28581998 | Common:1; Rare:39 |