| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:222424325-222424585 | Rare:78 | ||||
| chr2:222424909-222425307 | Rare:96 | ||||
| chr2:222655998-222656114 | Common:1; Rare:46 | ||||
| chr2:222656370-222656504 | Common:1; Rare:46 | ||||
| chr2:222860853-222861100 | Common:2; Rare:92 | ||||
| chr2:223837510-223837609 | Common:1; Rare:25 | ||||
| chr2:223837847-223838040 | Common:2; Rare:49 | ||||
| chr2:223945210-223945413 | Rare:92 | ||||
| chr2:223957181-223957538 | Common:4; Rare:133; Clinvar (benign):2 | ||||
| chr2:223957659-223957691 | Rare:13 | ||||
| chr2:224039222-224039415 | Rare:78 | ||||
| chr2:224584730-224585016 | Rare:96 | ||||
| chr2:224585299-224585523 | Common:3; Rare:93 | ||||
| chr2:224585788-224585964 | Rare:45 | ||||
| chr2:224947014-224947171 | Rare:21 |