| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156826158-156826327 | Common:3; Rare:58 | ||||
| chr3:157160043-157160285 | Rare:102 | ||||
| chr3:157543243-157543416 | Rare:39 | ||||
| chr3:158672527-158672721 | Common:2; Rare:53 | ||||
| chr3:158801997-158802178 | Common:2; Rare:84 | ||||
| chr3:160399196-160399307 | Rare:30; Clinvar:1 | ||||
| chr3:160676989-160677204 | Common:3; Rare:28 | ||||
| chr3:161105075-161105395 | Common:4; Rare:94 | ||||
| chr3:161221184-161221330 | Rare:46 | ||||
| chr3:167734837-167735239 | Common:4; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735458-167735763 | Common:1; Rare:71 | ||||
| chr3:168095879-168095999 | Rare:42 | ||||
| chr3:169146273-169146428 | Rare:36 | ||||
| chr3:169146518-169146584 | Rare:26 | ||||
| chr3:169662869-169663096 | Common:1; Rare:52 |