Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189661284-189661533 | Common:4; Rare:93 | ||||
chr2:189674400-189674749 | Common:2; Rare:85 | ||||
chr2:189783956-189784111 | Common:3; Rare:54; Clinvar (benign):1 | ||||
chr2:189784276-189784535 | Common:4; Rare:93; Clinvar:8; Clinvar (benign):2 | ||||
chr2:190319736-190319980 | Common:5; Rare:88; Clinvar (benign):5 | ||||
chr2:190534656-190534870 | Common:1; Rare:69 | ||||
chr2:190880588-190880853 | Common:4; Rare:90 | ||||
chr2:191014143-191014353 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191246162-191246243 | Rare:28 | ||||
chr2:191677833-191678211 | Common:4; Rare:106 | ||||
chr2:191678565-191678621 | Rare:25 | ||||
chr2:191846722-191846770 | Rare:14 | ||||
chr2:191847181-191847447 | Rare:38 | ||||
chr2:196068797-196068909 | Common:1; Rare:28 | ||||
chr2:196171501-196171851 | Common:1; Rare:106 |