| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49022009-49022167 | Rare:53; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr3:49104720-49104858 | Rare:65; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49132873-49132963 | Rare:21 | ||||
| chr3:49132969-49133088 | Rare:26; Clinvar:1 | ||||
| chr3:49339968-49340162 | Common:2; Rare:85 | ||||
| chr3:49357638-49357838 | Rare:69 | ||||
| chr3:49358163-49358486 | Common:4; Rare:169 | ||||
| chr3:49411839-49412428 | Common:2; Rare:210 | ||||
| chr3:49429255-49429363 | Rare:28 | ||||
| chr3:49674228-49674402 | Common:1; Rare:68 | ||||
| chr3:49689460-49689615 | Rare:47 | ||||
| chr3:49723930-49724007 | Common:2; Rare:31 | ||||
| chr3:50292347-50292659 | Common:1; Rare:137 | ||||
| chr3:50299329-50299683 | Common:1; Rare:87 | ||||
| chr3:50328161-50328323 | Rare:52 |