| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804416-42804657 | Common:2; Rare:71 | ||||
| chr3:43621907-43622312 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690817-43690995 | Common:3; Rare:96; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691556-43691668 | Common:1; Rare:18 | ||||
| chr3:44338079-44338206 | Common:2; Rare:45 | ||||
| chr3:44338316-44338489 | Common:2; Rare:58 | ||||
| chr3:44338675-44338807 | Common:3; Rare:48 | ||||
| chr3:44477641-44477715 | Common:1; Rare:18 | ||||
| chr3:44510588-44510661 | Common:2; Rare:23 | ||||
| chr3:44555111-44555263 | Rare:36 | ||||
| chr3:44624913-44625047 | Common:1; Rare:33 | ||||
| chr3:44729525-44729671 | Common:1; Rare:57 | ||||
| chr3:44761556-44761852 | Common:3; Rare:123 | ||||
| chr3:44861751-44861931 | Common:2; Rare:80 | ||||
| chr3:44976091-44976301 | Common:3; Rare:88 |