Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882168-179882311 | Common:1; Rare:26 | ||||
chr1:179882488-179882816 | Rare:157; Clinvar:7; Clinvar (benign):2 | ||||
chr1:180502529-180502696 | Rare:70 | ||||
chr1:182604391-182604569 | Rare:37 | ||||
chr1:182839019-182839399 | Common:2; Rare:127 | ||||
chr1:183186127-183186291 | Common:2; Rare:26; Clinvar (benign):2 | ||||
chr1:183472308-183472515 | Common:2; Rare:74 | ||||
chr1:183635655-183636040 | Common:2; Rare:106 | ||||
chr1:184386736-184387075 | Common:3; Rare:106 | ||||
chr1:185045253-185045611 | Common:2; Rare:122 | ||||
chr1:185156922-185157318 | Common:1; Rare:110 | ||||
chr1:185317193-185317468 | Common:1; Rare:82 | ||||
chr1:186375094-186375430 | Rare:97 | ||||
chr1:186375669-186375920 | Common:1; Rare:64 | ||||
chr1:186680421-186680627 | Common:2; Rare:46 |