| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:33718151-33718435 | Rare:116 | ||||
| chr3:33798271-33798732 | Common:3; Rare:132 | ||||
| chr3:33798833-33798934 | Rare:47 | ||||
| chr3:33798949-33799087 | Rare:46 | ||||
| chr3:36908072-36908181 | Common:1; Rare:18 | ||||
| chr3:36908440-36908579 | Common:1; Rare:30 | ||||
| chr3:36944460-36944577 | Rare:34 | ||||
| chr3:36944847-36945195 | Common:1; Rare:82 | ||||
| chr3:36992793-36992918 | Rare:40 | ||||
| chr3:36992941-36993602 | Common:3; Rare:222; Clinvar:39; Clinvar (benign):18; Clinvar (pathogenic):4 | ||||
| chr3:36993682-36993875 | Rare:75; Clinvar:1 | ||||
| chr3:37174796-37175031 | Common:1; Rare:51 | ||||
| chr3:37175515-37175570 | Common:1; Rare:13 | ||||
| chr3:37176051-37176145 | Common:1; Rare:31 | ||||
| chr3:37176222-37176717 | Common:1; Rare:143 |