| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12841416-12841890 | Common:2; Rare:141 | ||||
| chr3:12995019-12995201 | Common:1; Rare:46 | ||||
| chr3:13420192-13420534 | Common:1; Rare:106 | ||||
| chr3:13479922-13480324 | Common:3; Rare:103 | ||||
| chr3:14124177-14124472 | Common:3; Rare:69 | ||||
| chr3:14124725-14125150 | Common:4; Rare:120; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14177806-14178131 | Common:2; Rare:70 | ||||
| chr3:14178327-14178425 | Rare:28 | ||||
| chr3:14178478-14178936 | Common:3; Rare:223; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:14402341-14402745 | Common:3; Rare:97 | ||||
| chr3:14402806-14402939 | Rare:31 | ||||
| chr3:14402963-14403034 | Rare:12 | ||||
| chr3:14432310-14432532 | Common:1; Rare:38 | ||||
| chr3:14432668-14432742 | Common:1; Rare:17 | ||||
| chr3:14651367-14651841 | Common:1; Rare:150 |