Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:216683648-216683917 | Common:1; Rare:39 | ||||
chr2:216683947-216684057 | Rare:20 | ||||
chr2:216685356-216685378 | Rare:5 | ||||
chr2:216686048-216686144 | Rare:13 | ||||
chr2:217223393-217223752 | Common:4; Rare:61 | ||||
chr2:217805932-217806007 | Rare:13 | ||||
chr2:217806934-217807065 | Rare:24 | ||||
chr2:217966031-217966093 | Rare:13 | ||||
chr2:218254317-218254579 | Common:2; Rare:40 | ||||
chr2:218277368-218277669 | Rare:87 | ||||
chr2:218403122-218403284 | Common:3; Rare:66 | ||||
chr2:218572439-218572722 | Common:2; Rare:53 | ||||
chr2:219281769-219281975 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:219606774-219607101 | Rare:99 | ||||
chr2:221438872-221439000 | Common:1; Rare:17 |