| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99141135-99141787 | Common:3; Rare:231 | ||||
| chr2:99154863-99155063 | Common:2; Rare:81; Clinvar (benign):2 | ||||
| chr2:99180845-99181248 | Common:2; Rare:130 | ||||
| chr2:99337226-99337585 | Rare:124 | ||||
| chr2:99406383-99406671 | Rare:67 | ||||
| chr2:99489911-99490308 | Common:1; Rare:168 | ||||
| chr2:100562552-100563065 | Common:6; Rare:145 | ||||
| chr2:100924840-100925291 | Rare:84 | ||||
| chr2:101002162-101002322 | Rare:61 | ||||
| chr2:101151144-101151523 | Common:3; Rare:95 | ||||
| chr2:101252650-101252938 | Common:5; Rare:97 | ||||
| chr2:101253145-101253192 | Rare:21 | ||||
| chr2:101264689-101264911 | Rare:47 | ||||
| chr2:101308629-101308791 | Common:1; Rare:70 | ||||
| chr2:101839657-101840018 | Rare:63 |