Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228103207-228103494 | Common:1; Rare:111 | ||||
chr1:228109229-228109438 | Rare:65 | ||||
chr1:228139841-228140083 | Common:1; Rare:58 | ||||
chr1:228208477-228208560 | Common:1; Rare:10 | ||||
chr1:228416638-228416718 | Rare:17 | ||||
chr1:228457819-228458113 | Common:2; Rare:117 | ||||
chr1:229270986-229271331 | Rare:113 | ||||
chr1:229434005-229434270 | Common:4; Rare:65; Clinvar (benign):2 | ||||
chr1:229508178-229508449 | Common:1; Rare:107 | ||||
chr1:229625947-229626284 | Rare:113 | ||||
chr1:230642448-230642604 | Common:1; Rare:69 | ||||
chr1:230978745-230979144 | Common:2; Rare:156 | ||||
chr1:231241089-231241362 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337795-231338056 | Common:2; Rare:96 | ||||
chr1:231528488-231528758 | Common:2; Rare:90 |