Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:197499299-197499590 | Common:1; Rare:100 | ||||
chr2:197515926-197516144 | Rare:89 | ||||
chr2:197675707-197675863 | Rare:28 | ||||
chr2:197676027-197676057 | Rare:5 | ||||
chr2:197705206-197705468 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):3 | ||||
chr2:199911083-199911451 | Rare:125 | ||||
chr2:199955170-199955339 | Rare:35 | ||||
chr2:200305817-200306305 | Common:7; Rare:106 | ||||
chr2:200306312-200306919 | Common:5; Rare:171 | ||||
chr2:200510044-200510263 | Common:1; Rare:65 | ||||
chr2:200811808-200811993 | Rare:75 | ||||
chr2:200812272-200812500 | Common:5; Rare:79 | ||||
chr2:200864142-200864252 | Rare:45 | ||||
chr2:200864623-200864729 | Rare:31 | ||||
chr2:200889005-200889510 | Common:3; Rare:160 |