| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150408860-150409187 | Rare:83 | ||||
| chr3:150409374-150409582 | Rare:44 | ||||
| chr3:150469739-150469809 | Rare:9 | ||||
| chr3:151770114-151770461 | Common:4; Rare:56 | ||||
| chr3:152270025-152270094 | Rare:22 | ||||
| chr3:152270269-152270423 | Rare:22 | ||||
| chr3:152301731-152301828 | Rare:20 | ||||
| chr3:152456962-152457074 | Rare:18 | ||||
| chr3:155737861-155738050 | Common:1; Rare:19 | ||||
| chr3:156816986-156817166 | Rare:67 | ||||
| chr3:157174857-157175314 | Common:3; Rare:194 | ||||
| chr3:159824323-159824589 | Rare:49 | ||||
| chr3:169273391-169273564 | Rare:30 | ||||
| chr3:169764809-169764824 | Rare:4; Clinvar:1 | ||||
| chr3:169764835-169764880 | Rare:18; Clinvar:6; Clinvar (pathogenic):1 |