| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:231482860-231482949 | Rare:20 | ||||
| chr2:231514303-231514587 | Common:5; Rare:115 | ||||
| chr2:231559712-231559879 | Common:1; Rare:27 | ||||
| chr2:231712426-231712440 | Rare:4 | ||||
| chr2:231712605-231712875 | Common:2; Rare:85 | ||||
| chr2:231805834-231805869 | Rare:5 | ||||
| chr2:232050492-232050573 | Common:1; Rare:16 | ||||
| chr2:232131888-232131993 | Rare:13 | ||||
| chr2:232148778-232148907 | Rare:18 | ||||
| chr2:232553695-232553707 | Rare:2 | ||||
| chr2:232698967-232699115 | Rare:33 | ||||
| chr2:232700493-232700644 | Rare:26 | ||||
| chr2:232790842-232791078 | Rare:57 | ||||
| chr2:232844056-232844416 | Common:3; Rare:92; Clinvar (benign):1 | ||||
| chr2:233145428-233145709 | Common:2; Rare:43 |