| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43690634-43690993 | Common:6; Rare:152; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338331-44338797 | Common:8; Rare:155 | ||||
| chr3:44477655-44477695 | Rare:7 | ||||
| chr3:44510606-44510754 | Common:1; Rare:31 | ||||
| chr3:44624913-44625063 | Common:2; Rare:41 | ||||
| chr3:44729518-44729667 | Common:1; Rare:59 | ||||
| chr3:44761561-44761809 | Common:3; Rare:102 | ||||
| chr3:44861766-44861927 | Common:2; Rare:73 | ||||
| chr3:44976056-44976273 | Common:2; Rare:86 | ||||
| chr3:45146207-45146504 | Common:2; Rare:100 | ||||
| chr3:45388454-45388604 | Rare:36 | ||||
| chr3:45689180-45689459 | Common:1; Rare:93 | ||||
| chr3:45995809-45995961 | Common:2; Rare:33; Clinvar:1 | ||||
| chr3:46163437-46163458 | Rare:5 | ||||
| chr3:46693642-46693794 | Common:1; Rare:36 |