Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9003957-9004090 | Rare:56 | ||||
chr2:9423148-9423707 | Common:1; Rare:152 | ||||
chr2:9474431-9474623 | Common:7; Rare:70 | ||||
chr2:9555719-9555992 | Common:2; Rare:91 | ||||
chr2:9843154-9843553 | Common:7; Rare:122 | ||||
chr2:10689906-10690073 | Common:4; Rare:60 | ||||
chr2:11746500-11746661 | Common:2; Rare:50; Clinvar:3 | ||||
chr2:12716627-12717011 | Common:3; Rare:118 | ||||
chr2:15561294-15561412 | Rare:47 | ||||
chr2:17753699-17754168 | Common:4; Rare:146; Clinvar (benign):1 | ||||
chr2:18560673-18560801 | Rare:34 | ||||
chr2:19901668-19901792 | Common:1; Rare:67 | ||||
chr2:19901944-19902037 | Common:1; Rare:28 | ||||
chr2:19990058-19990217 | Rare:40 | ||||
chr2:20051475-20051834 | Common:1; Rare:106 |