Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:40370208-40370271 | Rare:14 | ||||
chr2:40370312-40370317 | Rare:1 | ||||
chr2:42290464-42290719 | Common:2; Rare:54 | ||||
chr2:42303111-42303336 | Common:1; Rare:80 | ||||
chr2:42315167-42315336 | Common:1; Rare:37 | ||||
chr2:42691270-42691342 | Rare:14 | ||||
chr2:43102919-43103019 | Common:2; Rare:14 | ||||
chr2:43896677-43896731 | Rare:15; Clinvar (benign):1 | ||||
chr2:43973675-43973876 | Rare:68; Clinvar:3; Clinvar (benign):4 | ||||
chr2:46076144-46076434 | Common:1; Rare:54 | ||||
chr2:46177563-46177710 | Common:1; Rare:29 | ||||
chr2:46556215-46556435 | Rare:43 | ||||
chr2:46699969-46700005 | Rare:6 | ||||
chr2:46700011-46700057 | Rare:8 | ||||
chr2:46707685-46707787 | Common:2; Rare:17 |