| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53255903-53256197 | Common:4; Rare:113 | ||||
| chr3:53347516-53347699 | Common:2; Rare:52 | ||||
| chr3:53846385-53846566 | Rare:59 | ||||
| chr3:53891794-53892040 | Common:2; Rare:76 | ||||
| chr3:56557086-56557234 | Common:2; Rare:58 | ||||
| chr3:56682822-56682911 | Common:2; Rare:35 | ||||
| chr3:56682919-56683358 | Common:4; Rare:153 | ||||
| chr3:57079247-57079375 | Common:2; Rare:44 | ||||
| chr3:57227600-57227922 | Common:4; Rare:107 | ||||
| chr3:57555996-57556339 | Rare:87 | ||||
| chr3:57597277-57597778 | Common:4; Rare:150 | ||||
| chr3:57692969-57693181 | Common:1; Rare:63 | ||||
| chr3:57756137-57756322 | Rare:46 | ||||
| chr3:57889876-57890129 | Rare:56; Clinvar (benign):2 | ||||
| chr3:57896720-57896932 | Common:1; Rare:46; Clinvar (benign):1 |