Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:95165647-95165829 | Rare:58 | ||||
chr2:95207434-95207538 | Rare:38 | ||||
chr2:95402607-95402757 | Rare:50 | ||||
chr2:96208248-96208422 | Rare:87 | ||||
chr2:96208793-96208942 | Common:3; Rare:57 | ||||
chr2:96265959-96266348 | Common:2; Rare:118; Clinvar:1 | ||||
chr2:96335707-96335831 | Common:2; Rare:44 | ||||
chr2:96638296-96638436 | Rare:36 | ||||
chr2:97645808-97646108 | Common:3; Rare:92 | ||||
chr2:97663902-97664247 | Common:1; Rare:110 | ||||
chr2:98608420-98608659 | Common:1; Rare:105; Clinvar (benign):1 | ||||
chr2:99154877-99155031 | Common:1; Rare:62 | ||||
chr2:99180956-99181233 | Common:2; Rare:84 | ||||
chr2:99337209-99337466 | Rare:89 | ||||
chr2:100562697-100563061 | Common:4; Rare:115 |