| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200812374-200812386 | Rare:4 | ||||
| chr2:200889005-200889439 | Common:3; Rare:141 | ||||
| chr2:200963630-200963903 | Common:1; Rare:67 | ||||
| chr2:201071626-201072039 | Rare:86 | ||||
| chr2:201451441-201451821 | Common:2; Rare:98 | ||||
| chr2:201642629-201642773 | Rare:69 | ||||
| chr2:201780890-201781202 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238498-202238627 | Rare:43 | ||||
| chr2:202265672-202265791 | Rare:42 | ||||
| chr2:202871650-202871674 | Rare:8 | ||||
| chr2:202911898-202912291 | Common:2; Rare:108 | ||||
| chr2:203238894-203239026 | Rare:51 | ||||
| chr2:203239221-203239364 | Rare:49 | ||||
| chr2:206085824-206085961 | Common:1; Rare:38 | ||||
| chr2:206159386-206159982 | Common:3; Rare:180 |