| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:220045323-220045919 | Common:2; Rare:113 | ||||
| chr1:220145145-220145253 | Common:1; Rare:21 | ||||
| chr1:220145515-220145840 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr1:220146642-220146682 | Rare:7 | ||||
| chr1:220155322-220155345 | Rare:1 | ||||
| chr1:220271698-220271837 | Common:1; Rare:41 | ||||
| chr1:220300505-220300802 | Common:1; Rare:60 | ||||
| chr1:220336495-220336613 | Rare:22 | ||||
| chr1:220337397-220337668 | Common:2; Rare:34 | ||||
| chr1:220370030-220370369 | Common:4; Rare:45 | ||||
| chr1:220370495-220370641 | Rare:27 | ||||
| chr1:220427134-220427327 | Rare:36 | ||||
| chr1:220733112-220733382 | Common:4; Rare:49 | ||||
| chr1:220882585-220882875 | Common:3; Rare:55 | ||||
| chr1:220957299-220957546 | Rare:45 |