| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:168249972-168250180 | Rare:54 | ||||
| chr3:169764949-169765222 | Common:1; Rare:104; Clinvar:7; Clinvar (pathogenic):5 | ||||
| chr3:170741298-170741590 | Rare:44 | ||||
| chr3:171806726-171806750 | Rare:3 | ||||
| chr3:171874281-171874557 | Common:3; Rare:47 | ||||
| chr3:172135785-172136026 | Rare:45 | ||||
| chr3:172138004-172138180 | Rare:30 | ||||
| chr3:172675694-172675732 | Rare:8 | ||||
| chr3:172749356-172749559 | Rare:34 | ||||
| chr3:175433144-175433364 | Common:1; Rare:50 | ||||
| chr3:177358390-177358780 | Common:3; Rare:89 | ||||
| chr3:177730777-177731104 | Common:3; Rare:61 | ||||
| chr3:182426495-182426643 | Rare:42 | ||||
| chr3:183285888-183286102 | Common:3; Rare:39 | ||||
| chr3:183447475-183447706 | Common:1; Rare:57 |