Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:223712352-223712698 | Common:2; Rare:118 | ||||
chr1:223845849-223846293 | Common:4; Rare:136 | ||||
chr1:223846371-223846550 | Common:2; Rare:43 | ||||
chr1:224113926-224114226 | Common:1; Rare:108 | ||||
chr1:224114533-224114742 | Common:2; Rare:62 | ||||
chr1:224182860-224183367 | Common:3; Rare:166 | ||||
chr1:224183623-224183724 | Rare:33 | ||||
chr1:224330057-224330581 | Common:8; Rare:193 | ||||
chr1:224356779-224356994 | Common:1; Rare:91 | ||||
chr1:224434729-224435135 | Common:1; Rare:106 | ||||
chr1:224435371-224435507 | Rare:22 | ||||
chr1:224929660-224929758 | Rare:40 | ||||
chr1:225427953-225428559 | Common:3; Rare:176; Clinvar:5; Clinvar (benign):3 | ||||
chr1:225428592-225428832 | Common:2; Rare:55 | ||||
chr1:225428844-225428967 | Rare:13 |