| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46211801-46212029 | Common:2; Rare:70 | ||||
| chr13:46387203-46387341 | Rare:37 | ||||
| chr13:46553026-46553252 | Common:2; Rare:76 | ||||
| chr13:46797123-46797357 | Common:2; Rare:80 | ||||
| chr13:46896841-46896973 | Rare:36 | ||||
| chr13:46897012-46897111 | Common:1; Rare:17 | ||||
| chr13:48001035-48001451 | Common:7; Rare:168; Clinvar:5; Clinvar (benign):11 | ||||
| chr13:48037645-48037820 | Common:2; Rare:84; Clinvar:2 | ||||
| chr13:48037971-48038074 | Common:2; Rare:20 | ||||
| chr13:48233036-48233184 | Common:3; Rare:37 | ||||
| chr13:48233271-48233475 | Common:2; Rare:68 | ||||
| chr13:48303683-48303728 | Rare:11; Clinvar (pathogenic):1 | ||||
| chr13:48532630-48532844 | Common:3; Rare:76 | ||||
| chr13:48533044-48533153 | Common:2; Rare:33 | ||||
| chr13:48975780-48975983 | Common:1; Rare:71 |