Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228139856-228140068 | Common:1; Rare:50 | ||||
chr1:228457865-228458113 | Common:1; Rare:78 | ||||
chr1:229271036-229271307 | Rare:90 | ||||
chr1:229508215-229508432 | Common:1; Rare:88 | ||||
chr1:229625964-229626269 | Rare:102 | ||||
chr1:230978762-230979108 | Common:2; Rare:132 | ||||
chr1:231241101-231241362 | Common:2; Rare:129; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337799-231338056 | Common:2; Rare:94 | ||||
chr1:231528515-231528738 | Common:2; Rare:79 | ||||
chr1:232950464-232950664 | Common:3; Rare:72 | ||||
chr1:234373342-234373588 | Common:1; Rare:121; Clinvar (benign):4 | ||||
chr1:234373642-234373768 | Rare:51; Clinvar (benign):3 | ||||
chr1:234608062-234608333 | Common:1; Rare:88 | ||||
chr1:236064931-236064963 | Rare:9 | ||||
chr1:236065037-236065296 | Common:2; Rare:104; Clinvar (pathogenic):1 |