Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70221278-70221541 | Rare:113 | ||||
chr1:70354664-70354856 | Rare:65 | ||||
chr1:71080963-71081383 | Rare:114 | ||||
chr1:74198148-74198333 | Common:2; Rare:107 | ||||
chr1:74673619-74673680 | Rare:14 | ||||
chr1:75724315-75724735 | Common:5; Rare:136; Clinvar:4; Clinvar (benign):4 | ||||
chr1:77219400-77219520 | Rare:54 | ||||
chr1:77683344-77683558 | Common:1; Rare:70 | ||||
chr1:77979000-77979292 | Common:2; Rare:106 | ||||
chr1:78649658-78649868 | Rare:35 | ||||
chr1:83998972-83999468 | Common:7; Rare:145 | ||||
chr1:84077871-84078141 | Common:1; Rare:103 | ||||
chr1:84690384-84690706 | Rare:103 | ||||
chr1:85276480-85276774 | Common:3; Rare:90 | ||||
chr1:85708341-85708506 | Common:2; Rare:55 |