| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183162770-183162863 | Common:2; Rare:19 | ||||
| chr3:183253039-183253306 | Common:3; Rare:77 | ||||
| chr3:183287308-183287736 | Common:7; Rare:69 | ||||
| chr3:183635516-183635682 | Common:1; Rare:53 | ||||
| chr3:183697652-183697896 | Common:2; Rare:107 | ||||
| chr3:184017842-184018103 | Common:2; Rare:84 | ||||
| chr3:184135221-184135394 | Common:2; Rare:53; Clinvar:5 | ||||
| chr3:184181786-184181996 | Rare:50 | ||||
| chr3:184185857-184186208 | Common:5; Rare:131 | ||||
| chr3:184248868-184249032 | Common:1; Rare:86; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249457-184249793 | Common:1; Rare:101 | ||||
| chr3:184298947-184299276 | Common:3; Rare:100 | ||||
| chr3:184314412-184314674 | Common:3; Rare:76 | ||||
| chr3:184315003-184315202 | Rare:47 | ||||
| chr3:184320118-184320300 | Rare:36 |