| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104708-49104951 | Rare:98; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49120743-49120968 | Rare:72 | ||||
| chr3:49132988-49133172 | Rare:38; Clinvar:1 | ||||
| chr3:49166296-49166453 | Common:1; Rare:38 | ||||
| chr3:49171020-49171330 | Common:1; Rare:59 | ||||
| chr3:49171428-49171636 | Common:3; Rare:44 | ||||
| chr3:49173380-49173780 | Common:3; Rare:65 | ||||
| chr3:49339990-49340327 | Common:3; Rare:116 | ||||
| chr3:49340681-49340795 | Rare:24 | ||||
| chr3:49358265-49358529 | Common:2; Rare:134 | ||||
| chr3:49358670-49358900 | Common:1; Rare:51 | ||||
| chr3:49411921-49412453 | Common:2; Rare:202 | ||||
| chr3:49422436-49422608 | Rare:87; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr3:49429256-49429461 | Common:1; Rare:43 | ||||
| chr3:49469854-49470319 | Common:1; Rare:133 |