| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47406506-47406749 | Rare:89 | ||||
| chr3:47501364-47501513 | Common:1; Rare:17 | ||||
| chr3:47849700-47850033 | Rare:125 | ||||
| chr3:47870850-47871285 | Common:1; Rare:125 | ||||
| chr3:48066435-48066445 | Rare:1 | ||||
| chr3:48529770-48529795 | Rare:3 | ||||
| chr3:48593373-48593575 | Rare:53; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr3:48680252-48680426 | Rare:26 | ||||
| chr3:48753177-48753324 | Common:1; Rare:26 | ||||
| chr3:48974855-48974929 | Rare:17 | ||||
| chr3:49026596-49026717 | Common:1; Rare:33 | ||||
| chr3:49101620-49101898 | Rare:86; Clinvar:3; Clinvar (benign):9 | ||||
| chr3:49130764-49131090 | Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:49280781-49281024 | Rare:50 | ||||
| chr3:49324697-49325005 | Common:1; Rare:63 |