| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45464627-45465190 | Common:2; Rare:275 | ||||
| chr13:45465200-45465560 | Common:2; Rare:144 | ||||
| chr13:46052584-46052920 | Common:6; Rare:219 | ||||
| chr13:46168260-46168860 | Common:6; Rare:102 | ||||
| chr13:46181903-46182032 | Rare:23 | ||||
| chr13:46182121-46182468 | Common:6; Rare:112 | ||||
| chr13:46211749-46212008 | Common:4; Rare:135 | ||||
| chr13:46387060-46387640 | Common:4; Rare:284 | ||||
| chr13:46552943-46553637 | Common:13; Rare:471 | ||||
| chr13:46796481-46796791 | Common:4; Rare:146 | ||||
| chr13:46796985-46797422 | Common:8; Rare:275 | ||||
| chr13:48000560-48001026 | Common:1; Rare:197 | ||||
| chr13:48001208-48001456 | Common:6; Rare:281; Clinvar:10; Clinvar (benign):16 | ||||
| chr13:48037586-48037816 | Common:6; Rare:292; Clinvar:6 | ||||
| chr13:48037841-48038152 | Common:15; Rare:258 |