| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:160241730-160241917 | Rare:32 | ||||
| chr2:160270299-160270623 | Common:2; Rare:79 | ||||
| chr2:160855942-160855984 | Common:1; Rare:13 | ||||
| chr2:161339870-161340112 | Rare:27 | ||||
| chr2:162317867-162317933 | Rare:22; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:164653124-164653390 | Common:2; Rare:42 | ||||
| chr2:164700551-164700940 | Common:3; Rare:93 | ||||
| chr2:164716041-164716099 | Rare:9 | ||||
| chr2:164743814-164744064 | Common:1; Rare:54 | ||||
| chr2:164787117-164787329 | Common:2; Rare:37 | ||||
| chr2:164839322-164839394 | Rare:14 | ||||
| chr2:164895278-164895549 | Common:2; Rare:47 | ||||
| chr2:164903438-164903456 | Rare:1 | ||||
| chr2:168247227-168247381 | Common:3; Rare:50 | ||||
| chr2:168705118-168705233 | Rare:22 |