| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42773178-42773342 | Common:1; Rare:51 | ||||
| chr3:42804403-42804663 | Common:2; Rare:76 | ||||
| chr3:43690817-43691028 | Common:4; Rare:118; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:43691537-43691650 | Common:1; Rare:20 | ||||
| chr3:44338094-44338200 | Common:2; Rare:38 | ||||
| chr3:44338335-44338518 | Common:3; Rare:66 | ||||
| chr3:44338668-44338810 | Common:3; Rare:51 | ||||
| chr3:44477637-44477780 | Common:1; Rare:31 | ||||
| chr3:44555100-44555217 | Rare:27 | ||||
| chr3:44624832-44625323 | Common:3; Rare:131 | ||||
| chr3:44761590-44761833 | Common:3; Rare:87 | ||||
| chr3:44861803-44861939 | Common:2; Rare:66 | ||||
| chr3:44975950-44976335 | Common:5; Rare:138 | ||||
| chr3:45689176-45689464 | Common:1; Rare:97 | ||||
| chr3:45995796-45995947 | Common:2; Rare:36; Clinvar:1 |