Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:190488538-190488818 | Rare:63 | ||||
chr2:196260214-196260257 | Rare:7 | ||||
chr2:197487876-197488144 | Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
chr2:197498694-197499071 | Common:7; Rare:106; Clinvar (benign):5 | ||||
chr2:199459312-199459493 | Common:1; Rare:47 | ||||
chr2:199459708-199459794 | Rare:24 | ||||
chr2:200590107-200590301 | Rare:30 | ||||
chr2:201644163-201644385 | Common:1; Rare:36 | ||||
chr2:202376072-202376229 | Rare:83 | ||||
chr2:205700617-205700819 | Common:2; Rare:51 | ||||
chr2:207163412-207163700 | Common:1; Rare:49 | ||||
chr2:215373322-215373682 | Common:3; Rare:83 | ||||
chr2:215378174-215378495 | Common:1; Rare:71; Clinvar:1 | ||||
chr2:216692157-216692192 | Rare:9 | ||||
chr2:217790308-217790528 | Common:1; Rare:37 |