Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:138501661-138502017 | Common:2; Rare:129 | ||||
chr2:144517331-144517578 | Rare:73; Clinvar:3; Clinvar (benign):4 | ||||
chr2:148020681-148021125 | Common:2; Rare:105; Clinvar (benign):2 | ||||
chr2:148021544-148021652 | Rare:21 | ||||
chr2:149587299-149587374 | Rare:19 | ||||
chr2:149587672-149587821 | Common:1; Rare:42; Clinvar:1 | ||||
chr2:151289592-151289734 | Common:1; Rare:35 | ||||
chr2:151828482-151828793 | Common:2; Rare:84 | ||||
chr2:152717829-152717947 | Rare:47 | ||||
chr2:152717975-152718050 | Rare:23 | ||||
chr2:152718267-152718654 | Common:2; Rare:144 | ||||
chr2:156332677-156332878 | Rare:60; Clinvar:2 | ||||
chr2:156436092-156436440 | Common:3; Rare:101 | ||||
chr2:158968416-158968728 | Rare:100 | ||||
chr2:159616418-159616567 | Common:1; Rare:30 |