Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:12277567-12277815 | Common:1; Rare:40 | ||||
chr2:12715909-12716084 | Common:2; Rare:35 | ||||
chr2:17544014-17544163 | Rare:26 | ||||
chr2:20447710-20448091 | Rare:122 | ||||
chr2:20448108-20448199 | Rare:27 | ||||
chr2:20448362-20448851 | Common:2; Rare:122 | ||||
chr2:20450931-20450952 | Rare:9 | ||||
chr2:20501309-20501551 | Common:19; Rare:102 | ||||
chr2:20641719-20641848 | Rare:29 | ||||
chr2:23523748-23523818 | Rare:19 | ||||
chr2:23524329-23524491 | Common:2; Rare:43 | ||||
chr2:24304201-24304440 | Common:1; Rare:39 | ||||
chr2:24310285-24310574 | Rare:86 | ||||
chr2:25822008-25822342 | Common:6; Rare:68 | ||||
chr2:26254288-26254472 | Rare:48; Clinvar (benign):2 |