| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183635497-183635707 | Common:3; Rare:65 | ||||
| chr3:183697680-183697917 | Common:2; Rare:105 | ||||
| chr3:183884813-183884959 | Rare:63 | ||||
| chr3:184017868-184018042 | Rare:46 | ||||
| chr3:184135219-184135413 | Common:2; Rare:60; Clinvar:5 | ||||
| chr3:184155271-184155336 | Rare:17 | ||||
| chr3:184181786-184181961 | Rare:44 | ||||
| chr3:184185863-184186210 | Common:5; Rare:130 | ||||
| chr3:184248864-184249015 | Rare:83; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249511-184249697 | Rare:49 | ||||
| chr3:184298944-184299338 | Common:5; Rare:120 | ||||
| chr3:184325270-184325578 | Common:1; Rare:81 | ||||
| chr3:184361603-184361770 | Rare:44 | ||||
| chr3:184362142-184362295 | Common:1; Rare:23 | ||||
| chr3:184711939-184712244 | Common:1; Rare:104 |