| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49131407-49131602 | Common:1; Rare:63; Clinvar:2 | ||||
| chr3:56935180-56935416 | Common:2; Rare:47 | ||||
| chr3:57952309-57952557 | Rare:39 | ||||
| chr3:64561052-64561349 | Common:10; Rare:52 | ||||
| chr3:75435060-75435395 | Common:4; Rare:117 | ||||
| chr3:75641103-75641279 | Rare:29 | ||||
| chr3:81761510-81761637 | Common:6; Rare:44; Clinvar (benign):1 | ||||
| chr3:101576970-101576991 | Common:1; Rare:1 | ||||
| chr3:101676275-101676509 | Common:1; Rare:81 | ||||
| chr3:101682817-101683153 | Common:1; Rare:60 | ||||
| chr3:107240630-107240764 | Rare:54 | ||||
| chr3:112420989-112421075 | Common:5; Rare:16 | ||||
| chr3:113285137-113285417 | Common:4; Rare:64 | ||||
| chr3:130111461-130111777 | Common:3; Rare:75 | ||||
| chr3:130112383-130112589 | Common:3; Rare:68 |