| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017168-61017286 | Common:3; Rare:30 | ||||
| chr2:61017318-61017819 | Common:3; Rare:392; Clinvar:13; Clinvar (benign):6 | ||||
| chr2:61065678-61066165 | Common:9; Rare:255 | ||||
| chr2:61066460-61066950 | Common:2; Rare:133 | ||||
| chr2:61144868-61145199 | Common:9; Rare:299 | ||||
| chr2:61177007-61177664 | Common:21; Rare:537 | ||||
| chr2:61177772-61178035 | Common:5; Rare:83 | ||||
| chr2:61178143-61179260 | Common:13; Rare:465 | ||||
| chr2:61184317-61185880 | Common:12; Rare:664 | ||||
| chr2:61470624-61471096 | Common:2; Rare:305 | ||||
| chr2:61471012-61471577 | Common:12; Rare:382 | ||||
| chr2:61536696-61536888 | Rare:63 | ||||
| chr2:61536910-61537330 | Common:2; Rare:154 | ||||
| chr2:61537530-61537920 | Common:4; Rare:250 | ||||
| chr2:61538090-61538553 | Common:3; Rare:280 |