| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32010410-32011270 | Common:6; Rare:922 | ||||
| chr2:32039347-32039747 | Rare:109 | ||||
| chr2:32039721-32040064 | Common:5; Rare:478 | ||||
| chr2:32039980-32041065 | Common:5; Rare:222 | ||||
| chr2:32062860-32063260 | Rare:96 | ||||
| chr2:32063273-32064122 | Common:11; Rare:1230; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):5 | ||||
| chr2:32064195-32064676 | Rare:227; Clinvar (benign):2 | ||||
| chr2:32165607-32166737 | Common:23; Rare:1015 | ||||
| chr2:32264667-32265129 | Common:2; Rare:183 | ||||
| chr2:32277640-32278290 | Common:8; Rare:593 | ||||
| chr2:32278310-32278630 | Common:5; Rare:157 | ||||
| chr2:32356395-32356795 | Common:3; Rare:153 | ||||
| chr2:32356710-32357370 | Common:37; Rare:1145 | ||||
| chr2:32357281-32357681 | Common:2; Rare:103 | ||||
| chr2:32627810-32628302 | Common:1; Rare:389 |