| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:189309726-189309920 | Common:1; Rare:45 | ||||
| chr3:190120885-190120957 | Rare:25 | ||||
| chr3:190322393-190322541 | Common:2; Rare:37 | ||||
| chr3:190513903-190514145 | Common:2; Rare:65 | ||||
| chr3:191329333-191329659 | Common:3; Rare:98 | ||||
| chr3:192917830-192917916 | Rare:46 | ||||
| chr3:193240992-193241325 | Common:4; Rare:113 | ||||
| chr3:193554806-193555036 | Common:1; Rare:54 | ||||
| chr3:193593081-193593388 | Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:194632718-194632935 | Common:2; Rare:38 | ||||
| chr3:195543209-195543475 | Common:3; Rare:100 | ||||
| chr3:195583885-195584397 | Common:12; Rare:105 | ||||
| chr3:195720865-195721006 | Common:3; Rare:25 | ||||
| chr3:195811769-195812154 | Common:7; Rare:100 | ||||
| chr3:195876656-195876932 | Common:3; Rare:113 |