| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:45689177-45689474 | Common:1; Rare:99 | ||||
| chr3:45943239-45943469 | Rare:42 | ||||
| chr3:45995723-45995882 | Rare:36; Clinvar:1 | ||||
| chr3:46407059-46407259 | Rare:37 | ||||
| chr3:46485086-46485379 | Common:1; Rare:51 | ||||
| chr3:46566105-46566475 | Rare:78 | ||||
| chr3:46612325-46612645 | Common:5; Rare:53 | ||||
| chr3:46693493-46693824 | Common:3; Rare:71 | ||||
| chr3:46811975-46812105 | Common:1; Rare:24 | ||||
| chr3:46812549-46812686 | Rare:34 | ||||
| chr3:46863404-46863661 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:46979511-46979846 | Common:2; Rare:81; Clinvar:1 | ||||
| chr3:46981971-46982208 | Rare:34 | ||||
| chr3:47163912-47164501 | Common:2; Rare:155 | ||||
| chr3:47380771-47381090 | Rare:107 |