| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:195657119-195657327 | Common:1; Rare:64 | ||||
| chr2:196171465-196171912 | Common:1; Rare:138 | ||||
| chr2:196926722-196926823 | Common:1; Rare:36 | ||||
| chr2:197434973-197435192 | Rare:75 | ||||
| chr2:197453244-197453571 | Rare:111 | ||||
| chr2:197497368-197497425 | Rare:10; Clinvar:1 | ||||
| chr2:197499808-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515968-197516087 | Rare:50 | ||||
| chr2:199457507-199457636 | Rare:28 | ||||
| chr2:200306147-200306562 | Common:5; Rare:97 | ||||
| chr2:200509913-200510210 | Common:1; Rare:106 | ||||
| chr2:200811437-200811588 | Common:1; Rare:53 | ||||
| chr2:200811743-200811964 | Rare:85 | ||||
| chr2:200864229-200864267 | Rare:14 | ||||
| chr2:200864542-200864818 | Common:1; Rare:100 |