Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228109194-228109471 | Rare:89 | ||||
chr1:228457866-228458107 | Common:1; Rare:73 | ||||
chr1:228487309-228487412 | Rare:40 | ||||
chr1:229271003-229271197 | Rare:72 | ||||
chr1:229625908-229626278 | Rare:123 | ||||
chr1:230978833-230979102 | Common:1; Rare:95 | ||||
chr1:231241088-231241362 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337772-231338049 | Common:3; Rare:108 | ||||
chr1:231528601-231528741 | Common:1; Rare:54 | ||||
chr1:234373365-234373840 | Common:2; Rare:214; Clinvar (benign):9 | ||||
chr1:235504385-235504694 | Common:5; Rare:95 | ||||
chr1:236604446-236604646 | Common:4; Rare:63 | ||||
chr1:241848141-241848244 | Common:1; Rare:20 | ||||
chr1:243255721-243256188 | Common:1; Rare:141; Clinvar:5; Clinvar (benign):1 | ||||
chr1:244864427-244864573 | Rare:51 |