| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12287706-12287995 | Common:8; Rare:60 | ||||
| chr3:12288936-12289113 | Common:1; Rare:37 | ||||
| chr3:12484365-12484560 | Common:2; Rare:59; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:12545475-12545824 | Common:3; Rare:75 | ||||
| chr3:12585728-12585926 | Rare:43; Clinvar (benign):2 | ||||
| chr3:12664002-12664300 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):5 | ||||
| chr3:13480040-13480339 | Common:2; Rare:70 | ||||
| chr3:14124685-14125190 | Common:4; Rare:148; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:14178448-14178881 | Common:3; Rare:210; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr3:14402437-14402770 | Common:3; Rare:72 | ||||
| chr3:14651486-14651869 | Rare:119 | ||||
| chr3:14947076-14947152 | Common:1; Rare:30 | ||||
| chr3:14947153-14947563 | Common:5; Rare:172 | ||||
| chr3:14948017-14948208 | Rare:86 | ||||
| chr3:14948354-14948673 | Common:2; Rare:99 |