Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:3558230-3558679 | Common:6; Rare:170 | ||||
chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
chr2:9423163-9423691 | Common:1; Rare:144 | ||||
chr2:9474491-9474630 | Common:6; Rare:63 | ||||
chr2:9555621-9555903 | Common:2; Rare:91 | ||||
chr2:9843250-9843515 | Common:6; Rare:76 | ||||
chr2:11465815-11465931 | Rare:52 | ||||
chr2:11466020-11466316 | Common:6; Rare:85 | ||||
chr2:11746556-11746682 | Common:2; Rare:48; Clinvar:5 | ||||
chr2:12716756-12717051 | Common:1; Rare:86 | ||||
chr2:17753721-17753897 | Common:2; Rare:64 | ||||
chr2:18560308-18560603 | Rare:115 | ||||
chr2:19990079-19990211 | Rare:34 | ||||
chr2:20350822-20351039 | Common:1; Rare:89 | ||||
chr2:20446851-20447118 | Common:4; Rare:118 |