| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:169812856-169813063 | Common:2; Rare:38 | ||||
| chr3:169982830-169983208 | Common:1; Rare:71 | ||||
| chr3:174440903-174441004 | Common:1; Rare:27 | ||||
| chr3:179604610-179604855 | Common:2; Rare:93 | ||||
| chr3:180989647-180989782 | Rare:59; Clinvar:1 | ||||
| chr3:184017856-184018098 | Common:1; Rare:77 | ||||
| chr3:184135260-184135416 | Common:2; Rare:46; Clinvar:2 | ||||
| chr3:184155116-184155501 | Rare:101 | ||||
| chr3:184248906-184249027 | Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:184249511-184249764 | Common:1; Rare:77 | ||||
| chr3:184305789-184306073 | Rare:70 | ||||
| chr3:184314394-184314654 | Common:3; Rare:78 | ||||
| chr3:184325051-184325372 | Common:2; Rare:75 | ||||
| chr3:184711981-184712202 | Common:1; Rare:81 | ||||
| chr3:185282873-185283008 | Common:1; Rare:35 |