Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153967435-153967508 | Common:1; Rare:7 | ||||
chr1:153967710-153967954 | Rare:47 | ||||
chr1:153986167-153986449 | Rare:73 | ||||
chr1:153990647-153990865 | Common:2; Rare:107 | ||||
chr1:154155014-154155129 | Common:1; Rare:43 | ||||
chr1:154182956-154183308 | Rare:113 | ||||
chr1:154183360-154183414 | Rare:6 | ||||
chr1:154192072-154192193 | Rare:21 | ||||
chr1:154206321-154206562 | Common:1; Rare:53 | ||||
chr1:154219843-154220220 | Common:5; Rare:106 | ||||
chr1:154220425-154221383 | Common:1; Rare:288 | ||||
chr1:154272555-154272785 | Common:4; Rare:63; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154321081-154321120 | Rare:8 | ||||
chr1:154325415-154325727 | Rare:103 | ||||
chr1:154328543-154328837 | Common:2; Rare:76 |