Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:75724271-75724634 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):3 | ||||
chr1:76074539-76074844 | Common:2; Rare:103 | ||||
chr1:77219400-77219536 | Rare:59 | ||||
chr1:77683315-77683565 | Common:1; Rare:81 | ||||
chr1:77779514-77779698 | Rare:56 | ||||
chr1:77888442-77888714 | Common:1; Rare:62; Clinvar:2 | ||||
chr1:77979013-77979319 | Common:2; Rare:103 | ||||
chr1:77979456-77979537 | Common:1; Rare:22 | ||||
chr1:78004547-78004954 | Common:4; Rare:94 | ||||
chr1:81306056-81306437 | Common:1; Rare:81 | ||||
chr1:81800344-81800431 | Rare:39 | ||||
chr1:81800778-81801010 | Common:3; Rare:84 | ||||
chr1:84077871-84078141 | Common:1; Rare:103 | ||||
chr1:84301602-84301713 | Rare:17 | ||||
chr1:84479202-84479302 | Common:2; Rare:51 |