| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197451141-197451181 | Common:1; Rare:10 | ||||
| chr2:197601867-197602130 | Common:1; Rare:42 | ||||
| chr2:197705911-197705984 | Rare:24; Clinvar (pathogenic):1 | ||||
| chr2:197838151-197838268 | Rare:26 | ||||
| chr2:198005350-198005511 | Rare:34 | ||||
| chr2:200307616-200307711 | Rare:33 | ||||
| chr2:200374195-200374349 | Common:1; Rare:26 | ||||
| chr2:200408620-200408650 | Rare:5 | ||||
| chr2:200482357-200482603 | Rare:36 | ||||
| chr2:200713181-200713431 | Rare:39 | ||||
| chr2:200757092-200757323 | Common:1; Rare:42 | ||||
| chr2:201117569-201117667 | Rare:17 | ||||
| chr2:201119549-201119655 | Rare:19 | ||||
| chr2:201120074-201120133 | |||||
| chr2:201123773-201124090 | Rare:45 |