Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:225427980-225428284 | Common:3; Rare:99; Clinvar:3; Clinvar (benign):2 | ||||
chr1:225777716-225777928 | Common:3; Rare:71 | ||||
chr1:225882320-225882402 | Rare:25 | ||||
chr1:225924248-225924443 | Common:5; Rare:48 | ||||
chr1:225999313-225999616 | Common:2; Rare:102 | ||||
chr1:226062052-226062094 | Rare:14 | ||||
chr1:226062504-226062798 | Rare:105 | ||||
chr1:226309135-226309474 | Common:1; Rare:149 | ||||
chr1:226939985-226940348 | Rare:124; Clinvar:3 | ||||
chr1:227735231-227735491 | Common:3; Rare:150 | ||||
chr1:228082412-228082765 | Common:5; Rare:136 | ||||
chr1:228103317-228103442 | Common:1; Rare:42 | ||||
chr1:228109223-228109468 | Rare:83 | ||||
chr1:228139876-228140083 | Common:1; Rare:50 | ||||
chr1:228425355-228425516 | Rare:53 |