| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219206690-219206923 | Rare:85 | ||||
| chr2:219229313-219229367 | Rare:14 | ||||
| chr2:219229541-219229899 | Common:2; Rare:114 | ||||
| chr2:219245383-219245542 | Common:1; Rare:49 | ||||
| chr2:219253867-219254222 | Common:2; Rare:86 | ||||
| chr2:219279207-219279567 | Common:3; Rare:109; Clinvar (benign):1 | ||||
| chr2:219498690-219498935 | Common:2; Rare:56 | ||||
| chr2:219543772-219544089 | Common:3; Rare:100 | ||||
| chr2:219552376-219552471 | Rare:25 | ||||
| chr2:219571511-219571605 | Rare:21 | ||||
| chr2:219572066-219572376 | Common:2; Rare:59 | ||||
| chr2:219597719-219597909 | Common:1; Rare:79 | ||||
| chr2:221572294-221572471 | Common:2; Rare:57 | ||||
| chr2:223052129-223052191 | Rare:12 | ||||
| chr2:223957257-223957474 | Common:4; Rare:81 |