Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:73385604-73386121 | Common:4; Rare:239; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr2:73386160-73386333 | Common:1; Rare:63; Clinvar (benign):3 | ||||
chr2:73736755-73736918 | Common:1; Rare:30 | ||||
chr2:73737223-73737582 | Common:3; Rare:117 | ||||
chr2:73780043-73780269 | Common:1; Rare:91 | ||||
chr2:73828794-73829057 | Common:2; Rare:61 | ||||
chr2:74002534-74002785 | Common:2; Rare:92 | ||||
chr2:74003171-74003219 | Common:2; Rare:18 | ||||
chr2:74147810-74148156 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr2:74148357-74148449 | Rare:23 | ||||
chr2:74178827-74179035 | Common:2; Rare:58 | ||||
chr2:74198290-74198637 | Common:10; Rare:113 | ||||
chr2:74369103-74369387 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):2 | ||||
chr2:74374584-74374816 | Rare:57 | ||||
chr2:74385441-74385545 | Rare:14 |