| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:126704095-126704278 | Common:2; Rare:50 | ||||
| chr3:127591081-127591249 | Common:1; Rare:39 | ||||
| chr3:127598209-127598446 | Common:3; Rare:64 | ||||
| chr3:127672808-127673028 | Common:4; Rare:106 | ||||
| chr3:127823169-127823340 | Common:3; Rare:34 | ||||
| chr3:128052186-128052500 | Common:2; Rare:105 | ||||
| chr3:128123731-128124031 | Rare:90 | ||||
| chr3:128650756-128651068 | Common:1; Rare:98 | ||||
| chr3:128725987-128726233 | Common:1; Rare:76; Clinvar:3 | ||||
| chr3:128879408-128879669 | Common:4; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161004-129161435 | Common:2; Rare:137 | ||||
| chr3:129183814-129184084 | Common:2; Rare:93 | ||||
| chr3:129249524-129249739 | Common:2; Rare:61 | ||||
| chr3:129439847-129440376 | Common:1; Rare:160; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129560548-129560667 | Rare:31 |