| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:33599195-33599445 | Common:1; Rare:96 | ||||
| chr2:36355500-36356099 | Common:4; Rare:208 | ||||
| chr2:36356233-36356618 | Common:2; Rare:154 | ||||
| chr2:36558435-36558681 | Common:2; Rare:67 | ||||
| chr2:36597875-36598075 | Common:5; Rare:88 | ||||
| chr2:37084276-37084563 | Common:3; Rare:108 | ||||
| chr2:37088183-37088439 | Common:1; Rare:55 | ||||
| chr2:37211841-37212384 | Common:3; Rare:163 | ||||
| chr2:37231413-37231753 | Common:5; Rare:174; Clinvar:1; Clinvar (benign):4 | ||||
| chr2:37324690-37324894 | Common:1; Rare:82 | ||||
| chr2:37671598-37671838 | Common:11; Rare:106 | ||||
| chr2:38076058-38076291 | Rare:61 | ||||
| chr2:38300578-38300622 | Rare:5 | ||||
| chr2:38665782-38666152 | Common:3; Rare:98 | ||||
| chr2:38746672-38746780 | Rare:36 |