Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156122560-156122702 | Rare:32 | ||||
chr1:156122934-156123205 | Common:3; Rare:52 | ||||
chr1:156123317-156123487 | Common:1; Rare:26 | ||||
chr1:156126167-156126612 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
chr1:156126721-156126876 | Rare:37 | ||||
chr1:156146916-156146943 | Rare:4 | ||||
chr1:156193554-156193613 | Rare:9 | ||||
chr1:156193682-156194189 | Common:3; Rare:117 | ||||
chr1:156212825-156212919 | Rare:22 | ||||
chr1:156212927-156213107 | Rare:67 | ||||
chr1:156213144-156213609 | Common:2; Rare:127 | ||||
chr1:156282211-156282633 | Common:2; Rare:100 | ||||
chr1:156282723-156283069 | Common:3; Rare:88 | ||||
chr1:156295607-156295752 | Common:1; Rare:49 | ||||
chr1:156337493-156337532 | Common:2; Rare:7 |