| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:184135199-184135389 | Common:2; Rare:58; Clinvar:5 | ||||
| chr3:184155297-184155618 | Common:1; Rare:104 | ||||
| chr3:184185856-184186223 | Common:5; Rare:141 | ||||
| chr3:184248875-184249021 | Rare:76; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249518-184249793 | Common:1; Rare:90 | ||||
| chr3:184298941-184299283 | Common:3; Rare:107 | ||||
| chr3:184314411-184314664 | Common:3; Rare:75 | ||||
| chr3:184361590-184361930 | Rare:77 | ||||
| chr3:184711330-184711525 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr3:184711791-184712395 | Common:3; Rare:175 | ||||
| chr3:185282844-185283023 | Common:1; Rare:43 | ||||
| chr3:185498848-185499191 | Rare:119 | ||||
| chr3:185552560-185552610 | Common:1; Rare:5 | ||||
| chr3:185585987-185586392 | Common:1; Rare:101 | ||||
| chr3:185824782-185825077 | Rare:81 |