| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150603126-150603510 | Common:3; Rare:141 | ||||
| chr3:152268570-152269392 | Common:2; Rare:282 | ||||
| chr3:152269443-152269731 | Rare:92 | ||||
| chr3:153162024-153162282 | Rare:85 | ||||
| chr3:155079425-155079683 | Common:6; Rare:61 | ||||
| chr3:155079790-155080040 | Common:1; Rare:62 | ||||
| chr3:155853239-155853478 | Rare:41; Clinvar:1 | ||||
| chr3:155853603-155853821 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:155854371-155854726 | Rare:100 | ||||
| chr3:155870315-155870680 | Common:2; Rare:108 | ||||
| chr3:156555010-156555229 | Common:1; Rare:105 | ||||
| chr3:156674356-156674744 | Common:3; Rare:106 | ||||
| chr3:157151021-157151257 | Rare:34 | ||||
| chr3:157152549-157152766 | Common:1; Rare:42 | ||||
| chr3:157158572-157158679 | Rare:23 |