| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15206019-15206274 | Rare:91 | ||||
| chr3:15427495-15427629 | Rare:47 | ||||
| chr3:15601512-15601804 | Common:4; Rare:123; Clinvar:1 | ||||
| chr3:15859807-15860114 | Common:4; Rare:97 | ||||
| chr3:16264882-16265243 | Common:2; Rare:119 | ||||
| chr3:17742534-17742665 | Common:2; Rare:48 | ||||
| chr3:19946974-19947412 | Common:5; Rare:164 | ||||
| chr3:20186137-20186415 | Common:4; Rare:90 | ||||
| chr3:23805812-23806049 | Common:1; Rare:50 | ||||
| chr3:23806889-23806999 | Common:1; Rare:30 | ||||
| chr3:23916905-23917231 | Rare:122 | ||||
| chr3:25783380-25783627 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr3:28241439-28241744 | Common:2; Rare:101 | ||||
| chr3:28348807-28349179 | Common:3; Rare:116 | ||||
| chr3:32502775-32502911 | Rare:42 |