Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:71376233-71376330 | Rare:18 | ||||
chr2:72649957-72650050 | Common:1; Rare:29 | ||||
chr2:73902240-73902428 | Common:2; Rare:39; Clinvar:1 | ||||
chr2:73929750-73929849 | Rare:15 | ||||
chr2:74369964-74370348 | Common:1; Rare:96; Clinvar:6; Clinvar (benign):1 | ||||
chr2:74370466-74370827 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
chr2:74377687-74378085 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:74918023-74918060 | Rare:3 | ||||
chr2:75239030-75239310 | Rare:68 | ||||
chr2:75239540-75239676 | Common:1; Rare:33 | ||||
chr2:75595800-75596007 | Common:1; Rare:41 | ||||
chr2:75664708-75664838 | Rare:42 | ||||
chr2:75676354-75676397 | Rare:3 | ||||
chr2:84439225-84439504 | Common:1; Rare:53 | ||||
chr2:84777763-84777863 | Rare:15 |