Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155662538-155662759 | Common:1; Rare:35 | ||||
chr1:156105121-156105249 | Rare:28 | ||||
chr1:156115921-156116093 | Rare:26 | ||||
chr1:156118368-156118538 | Common:2; Rare:25 | ||||
chr1:156120700-156120978 | Common:2; Rare:55 | ||||
chr1:156127605-156127828 | Common:3; Rare:35 | ||||
chr1:156130311-156130773 | Common:3; Rare:112; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156140248-156140304 | Rare:10 | ||||
chr1:156768139-156768170 | Rare:10 | ||||
chr1:160317030-160317302 | Common:2; Rare:50 | ||||
chr1:160406398-160406686 | Common:1; Rare:56 | ||||
chr1:160408083-160408360 | Common:1; Rare:54 | ||||
chr1:161020203-161020258 | Rare:12 | ||||
chr1:161051686-161051748 | Rare:21 | ||||
chr1:161084513-161084552 | Rare:10 |