Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882030-179882229 | Common:2; Rare:50 | ||||
chr1:179882240-179882397 | Rare:31 | ||||
chr1:179882412-179883210 | Common:4; Rare:345; Clinvar:11; Clinvar (benign):5 | ||||
chr1:179883223-179883411 | Common:1; Rare:40 | ||||
chr1:179954287-179954906 | Common:3; Rare:142 | ||||
chr1:179955133-179955267 | Common:1; Rare:30 | ||||
chr1:180154369-180154968 | Common:7; Rare:192 | ||||
chr1:180229863-180230039 | Common:4; Rare:74 | ||||
chr1:180502282-180503218 | Common:3; Rare:322 | ||||
chr1:180631847-180632211 | Common:5; Rare:133 | ||||
chr1:180632243-180632408 | Rare:44 | ||||
chr1:180912813-180913013 | Rare:44 | ||||
chr1:181022822-181023317 | Common:26; Rare:219 | ||||
chr1:181033228-181033467 | Common:2; Rare:42 | ||||
chr1:181033796-181034078 | Rare:67 |