| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:89821792-89821885 | Rare:25 | ||||
| chr1:89994981-89995178 | Common:2; Rare:75 | ||||
| chr1:91885955-91886070 | Rare:45 | ||||
| chr1:92298945-92299086 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:93179886-93179922 | Common:1; Rare:5 | ||||
| chr1:93180296-93180694 | Common:1; Rare:152 | ||||
| chr1:93345766-93345946 | Common:4; Rare:70 | ||||
| chr1:93447962-93448170 | Common:2; Rare:76 | ||||
| chr1:93879144-93879274 | Common:1; Rare:44 | ||||
| chr1:94418214-94418473 | Common:2; Rare:91 | ||||
| chr1:94541730-94541991 | Rare:76 | ||||
| chr1:94820149-94820454 | Common:4; Rare:79 | ||||
| chr1:94927028-94927464 | Common:3; Rare:144 | ||||
| chr1:95072889-95073252 | Common:4; Rare:108 | ||||
| chr1:95233945-95234231 | Common:5; Rare:83 |