Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228457559-228457647 | Rare:40 | ||||
chr1:228457654-228458318 | Common:2; Rare:342 | ||||
chr1:229271003-229271331 | Rare:108 | ||||
chr1:229508215-229508519 | Common:1; Rare:119 | ||||
chr1:229625947-229626299 | Rare:126 | ||||
chr1:230642230-230642581 | Common:1; Rare:118 | ||||
chr1:230978765-230979151 | Common:2; Rare:151 | ||||
chr1:231241094-231241356 | Common:2; Rare:126; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337819-231338088 | Common:3; Rare:93 | ||||
chr1:231528485-231528788 | Common:2; Rare:107 | ||||
chr1:232950453-232950674 | Common:3; Rare:81 | ||||
chr1:234373278-234373603 | Common:1; Rare:145; Clinvar (benign):4 | ||||
chr1:234373607-234373775 | Rare:70; Clinvar (benign):3 | ||||
chr1:235128708-235129112 | Common:1; Rare:165 | ||||
chr1:235328109-235328451 | Common:2; Rare:96 |