| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12288939-12289075 | Rare:29 | ||||
| chr3:12664084-12664300 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13480272-13480324 | Rare:22 | ||||
| chr3:14124738-14125173 | Common:4; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178870 | Common:2; Rare:155; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14402369-14402625 | Common:1; Rare:70 | ||||
| chr3:14651474-14651818 | Rare:102 | ||||
| chr3:14947233-14947569 | Common:4; Rare:154 | ||||
| chr3:14948033-14948208 | Rare:75 | ||||
| chr3:15205982-15206248 | Rare:88 | ||||
| chr3:15427471-15427623 | Common:1; Rare:57 | ||||
| chr3:15601516-15601804 | Common:4; Rare:121; Clinvar:1 | ||||
| chr3:15859800-15860099 | Common:4; Rare:89 | ||||
| chr3:16264921-16265243 | Common:2; Rare:92 | ||||
| chr3:17742596-17742952 | Common:4; Rare:124 |