Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:33476618-33476690 | Rare:15 | ||||
chr2:33599202-33599446 | Common:1; Rare:91 | ||||
chr2:36355419-36355731 | Common:1; Rare:103 | ||||
chr2:37084258-37084566 | Common:4; Rare:114 | ||||
chr2:37196394-37196669 | Common:3; Rare:96 | ||||
chr2:37231511-37231712 | Common:5; Rare:113; Clinvar (benign):3 | ||||
chr2:37324700-37324961 | Common:1; Rare:104 | ||||
chr2:37344515-37344762 | Common:2; Rare:83 | ||||
chr2:37671588-37671838 | Common:11; Rare:110 | ||||
chr2:37672519-37672718 | Common:4; Rare:68 | ||||
chr2:37925238-37925402 | Common:3; Rare:68 | ||||
chr2:37925407-37925549 | Rare:59 | ||||
chr2:38076138-38076291 | Rare:38 | ||||
chr2:38377200-38377509 | Common:3; Rare:134 | ||||
chr2:38602578-38603196 | Common:5; Rare:232 |