Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:218671969-218672339 | Common:2; Rare:93 | ||||
chr2:218782026-218782327 | Rare:93; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:219176898-219177119 | Common:4; Rare:67 | ||||
chr2:219206663-219206923 | Rare:93 | ||||
chr2:219229342-219229374 | Rare:10 | ||||
chr2:219229586-219229896 | Common:1; Rare:91 | ||||
chr2:219245378-219245511 | Rare:36 | ||||
chr2:219253894-219254056 | Common:1; Rare:52 | ||||
chr2:219279203-219279586 | Common:3; Rare:118; Clinvar (benign):1 | ||||
chr2:219498690-219498919 | Common:2; Rare:46 | ||||
chr2:219543735-219544103 | Common:3; Rare:112 | ||||
chr2:219552313-219552515 | Common:1; Rare:62 | ||||
chr2:219572066-219572361 | Common:2; Rare:54 | ||||
chr2:219597751-219597904 | Common:1; Rare:59 | ||||
chr2:221572271-221572448 | Common:2; Rare:65 |