Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231337743-231338314 | Common:5; Rare:187 | ||||
chr1:231528488-231528758 | Common:2; Rare:90 | ||||
chr1:232950503-232950669 | Common:1; Rare:57 | ||||
chr1:234373294-234373775 | Common:1; Rare:212; Clinvar (benign):7 | ||||
chr1:234608134-234608337 | Rare:70 | ||||
chr1:234609273-234609533 | Common:2; Rare:94 | ||||
chr1:235128620-235129078 | Common:1; Rare:183 | ||||
chr1:235327900-235328656 | Common:5; Rare:224 | ||||
chr1:235504378-235504741 | Common:5; Rare:115 | ||||
chr1:236604410-236604651 | Common:4; Rare:72 | ||||
chr1:236795234-236795457 | Common:1; Rare:108; Clinvar:4 | ||||
chr1:240091737-240092042 | Common:4; Rare:112 | ||||
chr1:241519591-241519977 | Common:3; Rare:124; Clinvar:16; Clinvar (benign):15; Clinvar (pathogenic):4 | ||||
chr1:241639821-241639975 | Rare:47 | ||||
chr1:241640236-241640558 | Common:7; Rare:119 |