Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:85539072-85539353 | Common:3; Rare:143; Clinvar (benign):7 | ||||
chr2:85561432-85561556 | Rare:47; Clinvar:4 | ||||
chr2:85595523-85595791 | Common:2; Rare:89 | ||||
chr2:85602651-85602867 | Rare:54 | ||||
chr2:85612030-85612098 | Rare:18 | ||||
chr2:85753558-85753881 | Common:2; Rare:92 | ||||
chr2:85888867-85889131 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):3 | ||||
chr2:86105805-86106270 | Common:3; Rare:146 | ||||
chr2:86195391-86195674 | Common:6; Rare:91 | ||||
chr2:86623831-86624024 | Common:2; Rare:85 | ||||
chr2:95165651-95165820 | Rare:49 | ||||
chr2:95207400-95207602 | Rare:81 | ||||
chr2:95402607-95402757 | Rare:50 | ||||
chr2:96208248-96208438 | Rare:92 | ||||
chr2:96208814-96208860 | Common:2; Rare:22 |