Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:88683962-88684350 | Common:3; Rare:115 | ||||
chr1:88992600-88992871 | Common:3; Rare:62 | ||||
chr1:89632894-89633202 | Common:1; Rare:88 | ||||
chr1:89994967-89995213 | Common:2; Rare:89 | ||||
chr1:91886088-91886340 | Rare:104 | ||||
chr1:92298934-92299074 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr1:93079077-93079290 | Common:2; Rare:92 | ||||
chr1:93180053-93180542 | Rare:175 | ||||
chr1:93345807-93345988 | Common:2; Rare:72 | ||||
chr1:93447996-93448177 | Common:2; Rare:67 | ||||
chr1:93847204-93847351 | Common:1; Rare:37 | ||||
chr1:93879083-93879299 | Common:2; Rare:83 | ||||
chr1:94541751-94541969 | Rare:69 | ||||
chr1:95072878-95073018 | Rare:54 | ||||
chr1:95233945-95234236 | Common:5; Rare:86 |