| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:177360637-177360674 | Common:1; Rare:4 | ||||
| chr3:178002236-178002404 | Rare:30 | ||||
| chr3:183447456-183447674 | Common:1; Rare:53 | ||||
| chr3:184229403-184229624 | Common:2; Rare:52 | ||||
| chr3:184710930-184711093 | Common:1; Rare:60 | ||||
| chr3:184711232-184711478 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chr3:185417864-185417939 | Rare:13 | ||||
| chr3:186521698-186521969 | Common:2; Rare:51 | ||||
| chr3:186772392-186772633 | Common:2; Rare:52 | ||||
| chr3:186772961-186773069 | Common:1; Rare:18 | ||||
| chr3:188948015-188948120 | Common:1; Rare:16 | ||||
| chr3:189460661-189460815 | Rare:26 | ||||
| chr3:191425379-191425553 | Common:2; Rare:44 | ||||
| chr3:194205788-194206023 | Rare:36 | ||||
| chr3:194583866-194584026 | Common:11; Rare:56 |