| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180679426-180679544 | Rare:21; Clinvar:3 | ||||
| chr3:180912567-180912730 | Common:1; Rare:55 | ||||
| chr3:180989652-180989804 | Rare:64; Clinvar:1 | ||||
| chr3:183099443-183099747 | Common:2; Rare:99; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183697652-183697916 | Common:2; Rare:113 | ||||
| chr3:183884828-183884959 | Rare:56 | ||||
| chr3:184017876-184018103 | Common:1; Rare:70 | ||||
| chr3:184135221-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184249515-184249689 | Rare:44 | ||||
| chr3:184298957-184299270 | Common:3; Rare:93 | ||||
| chr3:184335853-184335956 | Rare:34 | ||||
| chr3:184711939-184712243 | Common:1; Rare:103 | ||||
| chr3:185282855-185283030 | Common:1; Rare:42 | ||||
| chr3:185498900-185499181 | Rare:102 | ||||
| chr3:185585905-185586358 | Common:1; Rare:101 |