| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50569369-50569530 | Rare:41 | ||||
| chr22:50581345-50581455 | Rare:32; Clinvar:2 | ||||
| chr22:50723724-50723869 | Rare:35 | ||||
| chr3:4318801-4318814 | Common:1; Rare:2 | ||||
| chr3:4352494-4352726 | Common:1; Rare:39 | ||||
| chr3:4741761-4741925 | Rare:34 | ||||
| chr3:4750992-4751232 | Rare:62 | ||||
| chr3:4751598-4751801 | Common:3; Rare:43 | ||||
| chr3:4804563-4804854 | Common:2; Rare:57 | ||||
| chr3:4826005-4826092 | Rare:17 | ||||
| chr3:4981206-4981662 | Common:4; Rare:113 | ||||
| chr3:4981759-4982132 | Common:1; Rare:65 | ||||
| chr3:5022461-5022656 | Rare:40 | ||||
| chr3:5023241-5023689 | Common:4; Rare:107 | ||||
| chr3:5026666-5026909 | Common:3; Rare:54 |