Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:168456543-168456833 | Rare:96 | ||||
chr2:169479348-169479547 | Common:3; Rare:67; Clinvar (benign):1 | ||||
chr2:169584268-169584630 | Common:1; Rare:134 | ||||
chr2:169584703-169584819 | Rare:31 | ||||
chr2:169694323-169694590 | Common:6; Rare:98 | ||||
chr2:169733589-169734023 | Common:4; Rare:112 | ||||
chr2:169824813-169824988 | Common:2; Rare:60 | ||||
chr2:170815569-170815701 | Common:1; Rare:34 | ||||
chr2:170815981-170816187 | Common:5; Rare:46 | ||||
chr2:170816460-170816752 | Common:4; Rare:66; Clinvar:1 | ||||
chr2:170928873-170929343 | Common:5; Rare:138 | ||||
chr2:171159212-171159353 | Rare:34 | ||||
chr2:171159638-171159918 | Rare:73 | ||||
chr2:171160160-171160266 | Common:5; Rare:32 | ||||
chr2:171160292-171160764 | Common:5; Rare:180 |