| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:160399478-160399700 | Rare:63; Clinvar:2 | ||||
| chr3:160400136-160400238 | Rare:21 | ||||
| chr3:160449508-160449993 | Common:2; Rare:137 | ||||
| chr3:160565406-160565831 | Common:2; Rare:153 | ||||
| chr3:160755442-160755625 | Common:1; Rare:65 | ||||
| chr3:161105071-161105367 | Common:3; Rare:85 | ||||
| chr3:161221196-161221389 | Common:2; Rare:62 | ||||
| chr3:167734800-167735280 | Common:5; Rare:155; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735611-167735778 | Rare:44; Clinvar:1 | ||||
| chr3:168094777-168094872 | Rare:18 | ||||
| chr3:168095088-168095444 | Rare:114 | ||||
| chr3:169147035-169147248 | Rare:46 | ||||
| chr3:169769554-169769610 | Rare:23 | ||||
| chr3:169772748-169772838 | Rare:21 | ||||
| chr3:169773305-169773424 | Rare:43 |