| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41201366-41202105 | Common:2; Rare:138 | ||||
| chr3:41203069-41203407 | Common:2; Rare:59 | ||||
| chr3:41205997-41206242 | Rare:41 | ||||
| chr3:41207922-41208051 | Rare:18 | ||||
| chr3:41212818-41213276 | Common:1; Rare:84 | ||||
| chr3:41214427-41214724 | Common:2; Rare:44 | ||||
| chr3:41215002-41215163 | Rare:27 | ||||
| chr3:41215223-41215256 | Rare:2 | ||||
| chr3:41215413-41215739 | Common:2; Rare:61 | ||||
| chr3:41218809-41218874 | Common:1; Rare:8 | ||||
| chr3:41219145-41219444 | Rare:49 | ||||
| chr3:41219521-41219926 | Common:1; Rare:77 | ||||
| chr3:41220405-41220730 | Common:1; Rare:60 | ||||
| chr3:41221100-41221346 | Common:1; Rare:51 | ||||
| chr3:41224949-41225694 | Rare:162; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 |