Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:190534688-190534853 | Common:1; Rare:56 | ||||
chr2:190880595-190880882 | Common:4; Rare:100 | ||||
chr2:191014133-191014353 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677856-191678173 | Common:4; Rare:91 | ||||
chr2:197434980-197435276 | Rare:94 | ||||
chr2:197453249-197453556 | Rare:104 | ||||
chr2:197499807-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
chr2:197515890-197516098 | Common:1; Rare:83 | ||||
chr2:200811366-200811572 | Common:1; Rare:67 | ||||
chr2:200811811-200811938 | Rare:50 | ||||
chr2:200889278-200889439 | Common:2; Rare:64 | ||||
chr2:200963635-200963915 | Common:1; Rare:70 | ||||
chr2:201071586-201072008 | Rare:91 | ||||
chr2:201115974-201116196 | Common:2; Rare:40 | ||||
chr2:201116212-201116361 | Rare:24 |