| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206085772-206085960 | Common:1; Rare:54 | ||||
| chr2:206086229-206086303 | Rare:10 | ||||
| chr2:206159190-206160160 | Common:7; Rare:290; Clinvar (benign):2 | ||||
| chr2:206274495-206274768 | Common:1; Rare:81 | ||||
| chr2:206274841-206275079 | Common:1; Rare:71 | ||||
| chr2:206443318-206443544 | Common:1; Rare:74 | ||||
| chr2:206765249-206765382 | Common:1; Rare:49 | ||||
| chr2:206765518-206765661 | Common:2; Rare:43; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207166847-207166947 | Rare:46 | ||||
| chr2:207529657-207530119 | Common:3; Rare:127 | ||||
| chr2:207558815-207559192 | Common:3; Rare:79 | ||||
| chr2:207625226-207625417 | Common:1; Rare:55 | ||||
| chr2:207711276-207711539 | Common:1; Rare:77 | ||||
| chr2:207711589-207712016 | Common:2; Rare:130 | ||||
| chr2:207712160-207712232 | Rare:22 |