| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200509867-200510141 | Common:1; Rare:101 | ||||
| chr2:200585924-200586116 | Rare:53 | ||||
| chr2:200811432-200811617 | Common:1; Rare:69 | ||||
| chr2:200864190-200864272 | Rare:33 | ||||
| chr2:200864552-200864811 | Common:1; Rare:93 | ||||
| chr2:200888989-200889445 | Common:3; Rare:143 | ||||
| chr2:200963400-200963436 | Rare:8 | ||||
| chr2:200963453-200963871 | Common:1; Rare:106 | ||||
| chr2:201071569-201072047 | Rare:108 | ||||
| chr2:201115811-201116473 | Common:2; Rare:128 | ||||
| chr2:201117406-201117608 | Rare:23 | ||||
| chr2:201118429-201118877 | Rare:68 | ||||
| chr2:201132659-201132848 | Rare:23 | ||||
| chr2:201182996-201183203 | Common:1; Rare:31; Clinvar (benign):2 | ||||
| chr2:201233329-201233548 | Common:1; Rare:41 |