| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46085861-46086016 | Common:1; Rare:35 | ||||
| chr22:47631624-47631815 | Common:2; Rare:54 | ||||
| chr22:49657460-49657628 | Common:2; Rare:67 | ||||
| chr3:4831311-4831578 | Common:3; Rare:46 | ||||
| chr3:6179814-6180027 | Common:2; Rare:49 | ||||
| chr3:6490686-6490839 | Common:5; Rare:59 | ||||
| chr3:9396117-9396322 | Rare:67 | ||||
| chr3:30292364-30292629 | Rare:49 | ||||
| chr3:31004482-31004539 | Rare:9 | ||||
| chr3:32420210-32420582 | Common:1; Rare:54 | ||||
| chr3:37163350-37163528 | Common:1; Rare:28 | ||||
| chr3:38455427-38455549 | Common:1; Rare:24 | ||||
| chr3:39411647-39411960 | Common:1; Rare:83; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:40453171-40453417 | Common:5; Rare:53 | ||||
| chr3:42652728-42652953 | Rare:44 |