| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10026283-10026432 | Common:1; Rare:52 | ||||
| chr3:11154390-11154531 | Common:3; Rare:40 | ||||
| chr3:12663821-12663913 | Rare:25; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:14124707-14125184 | Common:4; Rare:143; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178524-14178860 | Common:2; Rare:173; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651483-14651793 | Rare:87 | ||||
| chr3:14947221-14947551 | Common:4; Rare:145 | ||||
| chr3:15065240-15065362 | Common:2; Rare:43 | ||||
| chr3:15206057-15206294 | Common:1; Rare:96 | ||||
| chr3:15427478-15427623 | Common:1; Rare:51 | ||||
| chr3:15601469-15601775 | Common:4; Rare:124; Clinvar:1 | ||||
| chr3:16264820-16265249 | Common:2; Rare:149 | ||||
| chr3:16513618-16513801 | Common:4; Rare:45 | ||||
| chr3:19947037-19947399 | Common:4; Rare:133 | ||||
| chr3:23202813-23203191 | Common:1; Rare:124 |