Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189783956-189784125 | Common:3; Rare:62; Clinvar (benign):1 | ||||
chr2:189784281-189784537 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190343845-190344031 | Rare:39 | ||||
chr2:191014124-191014446 | Common:3; Rare:109; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677856-191678161 | Common:4; Rare:86 | ||||
chr2:191678565-191678597 | Rare:15 | ||||
chr2:197434970-197435192 | Rare:75 | ||||
chr2:197499792-197499997 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr2:197500052-197500191 | Rare:42 | ||||
chr2:197500193-197500430 | Common:1; Rare:99 | ||||
chr2:199851113-199851265 | Common:1; Rare:62 | ||||
chr2:200509913-200510127 | Common:1; Rare:79 | ||||
chr2:200811308-200811614 | Common:1; Rare:98 | ||||
chr2:200811804-200812012 | Rare:85 | ||||
chr2:200864198-200864268 | Rare:28 |