Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:219279646-219279812 | Common:1; Rare:48; Clinvar (benign):3 | ||||
chr2:219498692-219498929 | Common:2; Rare:51 | ||||
chr2:219543778-219544044 | Common:3; Rare:87 | ||||
chr2:219571444-219571605 | Rare:38 | ||||
chr2:219598061-219598122 | Common:1; Rare:32 | ||||
chr2:224039226-224039368 | Rare:63 | ||||
chr2:224402097-224402249 | Common:1; Rare:27 | ||||
chr2:226836358-226836539 | Common:3; Rare:51 | ||||
chr2:227325207-227325355 | Common:4; Rare:49 | ||||
chr2:229921943-229922264 | Common:2; Rare:129 | ||||
chr2:229922426-229922506 | Rare:21 | ||||
chr2:230219921-230220024 | Rare:16 | ||||
chr2:231464337-231464725 | Common:3; Rare:134 | ||||
chr2:231706468-231706661 | Common:2; Rare:42 | ||||
chr2:231708379-231708568 | Rare:72 |