| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73779829-73780303 | Common:2; Rare:196 | ||||
| chr2:73828733-73829168 | Common:2; Rare:97 | ||||
| chr2:73829288-73829552 | Common:4; Rare:63 | ||||
| chr2:73926676-73927089 | Common:2; Rare:183; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr2:73927095-73927159 | Rare:11 | ||||
| chr2:73927195-73927326 | Rare:26 | ||||
| chr2:73985521-73986006 | Common:4; Rare:118 | ||||
| chr2:73986297-73986456 | Rare:19 | ||||
| chr2:74002523-74002728 | Common:2; Rare:78 | ||||
| chr2:74147600-74147704 | Rare:18 | ||||
| chr2:74147816-74148168 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:74178191-74178563 | Rare:67 | ||||
| chr2:74178755-74179104 | Common:5; Rare:106 | ||||
| chr2:74198307-74198735 | Common:7; Rare:162 | ||||
| chr2:74198950-74199364 | Common:2; Rare:96 |