| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:146544465-146544827 | Common:5; Rare:87 | ||||
| chr3:146544835-146544897 | Rare:15 | ||||
| chr3:148991386-148991643 | Common:2; Rare:115; Clinvar (benign):1 | ||||
| chr3:149086478-149086709 | Rare:69 | ||||
| chr3:149129545-149129713 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149333228-149333541 | Common:4; Rare:86 | ||||
| chr3:149375307-149375623 | Common:1; Rare:79 | ||||
| chr3:149377373-149377469 | Rare:32 | ||||
| chr3:149377473-149377837 | Common:1; Rare:100 | ||||
| chr3:149657904-149658170 | Common:1; Rare:55 | ||||
| chr3:149752415-149752579 | Common:2; Rare:59 | ||||
| chr3:149813037-149813344 | Common:1; Rare:102 | ||||
| chr3:149813470-149813501 | Rare:5 | ||||
| chr3:149895186-149895514 | Common:3; Rare:50 | ||||
| chr3:150408170-150408320 | Common:2; Rare:59 |