| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43879705-43879879 | Common:18; Rare:56 | ||||
| chr13:44373405-44373704 | Rare:68 | ||||
| chr13:44435170-44435447 | Common:3; Rare:79 | ||||
| chr13:44436685-44436723 | Rare:6 | ||||
| chr13:44436760-44437033 | Common:2; Rare:85 | ||||
| chr13:44989443-44989634 | Rare:75 | ||||
| chr13:45120180-45120596 | Common:2; Rare:101 | ||||
| chr13:45341036-45341624 | Common:4; Rare:264 | ||||
| chr13:45464738-45465042 | Common:1; Rare:78 | ||||
| chr13:46052561-46052821 | Common:2; Rare:67 | ||||
| chr13:46387235-46387352 | Rare:28 | ||||
| chr13:46797115-46797317 | Common:3; Rare:73 | ||||
| chr13:48037703-48037789 | Common:1; Rare:45 | ||||
| chr13:48233060-48233475 | Common:3; Rare:144 | ||||
| chr13:48303674-48304016 | Common:1; Rare:116; Clinvar:12; Clinvar (benign):6; Clinvar (pathogenic):2 |