| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48504152-48504281 | Common:2; Rare:35 | ||||
| chr3:48556778-48557173 | Common:1; Rare:91 | ||||
| chr3:48635459-48635627 | Rare:51 | ||||
| chr3:48847663-48847969 | Common:1; Rare:84 | ||||
| chr3:48918793-48918940 | Common:2; Rare:87 | ||||
| chr3:49007184-49007426 | Common:2; Rare:94 | ||||
| chr3:49021502-49021646 | Rare:40 | ||||
| chr3:49021901-49022167 | Rare:77; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr3:49104729-49104913 | Rare:76; Clinvar (benign):3 | ||||
| chr3:49120773-49120978 | Rare:65 | ||||
| chr3:49132976-49133148 | Rare:38; Clinvar:2 | ||||
| chr3:49166289-49166451 | Common:1; Rare:41 | ||||
| chr3:49340020-49340311 | Common:3; Rare:96 | ||||
| chr3:49358255-49358550 | Common:3; Rare:146 | ||||
| chr3:49411894-49412213 | Common:1; Rare:111 |