| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49028249-49028489 | Rare:73 | ||||
| chr3:49094023-49094287 | Rare:60 | ||||
| chr3:49104471-49104568 | Rare:36; Clinvar (benign):2 | ||||
| chr3:49104692-49104910 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:49120754-49121027 | Rare:80 | ||||
| chr3:49132988-49133161 | Rare:36; Clinvar:1 | ||||
| chr3:49166293-49166442 | Common:1; Rare:38 | ||||
| chr3:49340013-49340221 | Common:2; Rare:79 | ||||
| chr3:49358205-49358458 | Common:4; Rare:136 | ||||
| chr3:49411857-49412214 | Common:1; Rare:120 | ||||
| chr3:49429262-49429419 | Rare:34 | ||||
| chr3:49674218-49674418 | Common:1; Rare:77 | ||||
| chr3:49723937-49724214 | Common:8; Rare:94 | ||||
| chr3:49786501-49786781 | Rare:88 | ||||
| chr3:49856521-49856668 | Common:1; Rare:34 |