| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96642624-96642799 | Rare:38 | ||||
| chr2:96740033-96740289 | Common:5; Rare:63 | ||||
| chr2:96816037-96816266 | Common:3; Rare:86 | ||||
| chr2:96857888-96858239 | Common:2; Rare:127 | ||||
| chr2:96869393-96869631 | Common:2; Rare:59 | ||||
| chr2:97094806-97094973 | Common:1; Rare:38 | ||||
| chr2:97113023-97113292 | Common:1; Rare:67 | ||||
| chr2:97113454-97113756 | Common:2; Rare:86 | ||||
| chr2:97590215-97590370 | Common:1; Rare:33 | ||||
| chr2:97645806-97646108 | Common:3; Rare:93 | ||||
| chr2:97663897-97664296 | Common:1; Rare:124 | ||||
| chr2:98608407-98608665 | Common:1; Rare:113; Clinvar (benign):1 | ||||
| chr2:99141128-99141766 | Common:3; Rare:231 | ||||
| chr2:99154855-99155094 | Common:3; Rare:100; Clinvar (benign):3 | ||||
| chr2:99180962-99181239 | Common:2; Rare:83 |