Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159923314-159923482 | Rare:40 | ||||
chr1:159925456-159925617 | Common:1; Rare:42 | ||||
chr1:160031950-160032060 | Rare:31 | ||||
chr1:160098852-160099109 | Common:2; Rare:38 | ||||
chr1:160115560-160115819 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
chr1:160190244-160190413 | Common:1; Rare:43 | ||||
chr1:160190474-160190597 | Common:1; Rare:26 | ||||
chr1:160262111-160262243 | Rare:36 | ||||
chr1:160262417-160262634 | Common:1; Rare:67 | ||||
chr1:160343148-160343421 | Rare:107 | ||||
chr1:160400410-160400608 | Common:1; Rare:51 | ||||
chr1:161038903-161039019 | Common:1; Rare:43 | ||||
chr1:161045878-161046083 | Common:1; Rare:56 | ||||
chr1:161117982-161118141 | Rare:83 | ||||
chr1:161132417-161132705 | Common:1; Rare:95 |