| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45340665-45341065 | Common:4; Rare:225 | ||||
| chr13:45341152-45341513 | Common:4; Rare:178 | ||||
| chr13:45417603-45418043 | Common:3; Rare:100 | ||||
| chr13:45418360-45418650 | Common:1; Rare:77 | ||||
| chr13:45464628-45464949 | Common:1; Rare:70 | ||||
| chr13:45465171-45465583 | Common:1; Rare:141 | ||||
| chr13:45615560-45615863 | Rare:78 | ||||
| chr13:46052718-46052907 | Common:2; Rare:58 | ||||
| chr13:46387120-46387555 | Common:3; Rare:202 | ||||
| chr13:46552964-46553204 | Common:2; Rare:88 | ||||
| chr13:46797069-46797419 | Common:3; Rare:106 | ||||
| chr13:48001271-48001482 | Common:3; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:48037596-48037795 | Common:1; Rare:90 | ||||
| chr13:48037936-48038160 | Common:5; Rare:60 | ||||
| chr13:48095028-48095282 | Common:2; Rare:122 |