| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191246162-191246351 | Common:1; Rare:49 | ||||
| chr2:191263168-191263388 | Rare:36 | ||||
| chr2:191677856-191678194 | Common:4; Rare:96 | ||||
| chr2:197434970-197435192 | Rare:75 | ||||
| chr2:197453151-197453576 | Rare:146 | ||||
| chr2:197453874-197454011 | Rare:40 | ||||
| chr2:197499773-197500446 | Common:2; Rare:257; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:197515861-197516089 | Common:1; Rare:90 | ||||
| chr2:197705212-197705463 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:199851115-199851204 | Common:1; Rare:45 | ||||
| chr2:200509926-200510199 | Common:1; Rare:95 | ||||
| chr2:200585866-200586166 | Rare:85 | ||||
| chr2:200811286-200811614 | Common:1; Rare:104 | ||||
| chr2:200864229-200864252 | Rare:6 | ||||
| chr2:200864571-200864828 | Common:1; Rare:96 |