| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12484365-12484554 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12664058-12664300 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:12841493-12841621 | Common:1; Rare:61 | ||||
| chr3:13480018-13480330 | Common:2; Rare:77 | ||||
| chr3:14124746-14125099 | Common:4; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178565-14178873 | Common:2; Rare:160; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14402395-14402622 | Common:1; Rare:63 | ||||
| chr3:14947211-14947583 | Common:4; Rare:165 | ||||
| chr3:14948422-14948637 | Common:2; Rare:62 | ||||
| chr3:15065178-15065394 | Common:2; Rare:82 | ||||
| chr3:15099127-15099299 | Rare:43 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15601506-15601810 | Common:4; Rare:128; Clinvar:2 | ||||
| chr3:15859787-15860114 | Common:4; Rare:103 | ||||
| chr3:16264921-16265220 | Common:2; Rare:82 |