| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51385025-51385299 | Rare:77 | ||||
| chr3:51499950-51500038 | Rare:22 | ||||
| chr3:51671070-51671284 | Common:2; Rare:69 | ||||
| chr3:51975046-51975136 | Common:1; Rare:33 | ||||
| chr3:51983310-51983511 | Rare:47 | ||||
| chr3:52154394-52154521 | Rare:28 | ||||
| chr3:52225593-52225838 | Rare:51 | ||||
| chr3:52239069-52239282 | Common:2; Rare:74 | ||||
| chr3:52287539-52287844 | Common:3; Rare:76 | ||||
| chr3:52455406-52455644 | Common:2; Rare:77 | ||||
| chr3:52685772-52686072 | Common:3; Rare:108 | ||||
| chr3:52705787-52706252 | Common:2; Rare:167 | ||||
| chr3:52770916-52771112 | Common:3; Rare:64 | ||||
| chr3:53130402-53130568 | Common:1; Rare:56; Clinvar (benign):3 | ||||
| chr3:53347525-53347685 | Common:1; Rare:45 |