| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46553026-46553389 | Common:4; Rare:111 | ||||
| chr13:46797099-46797291 | Common:3; Rare:69 | ||||
| chr13:48001183-48001383 | Common:1; Rare:93; Clinvar:5; Clinvar (benign):11 | ||||
| chr13:48037610-48037771 | Rare:68 | ||||
| chr13:48037918-48038045 | Common:4; Rare:44 | ||||
| chr13:48095070-48095235 | Common:1; Rare:80 | ||||
| chr13:48233066-48233475 | Common:3; Rare:143 | ||||
| chr13:48303657-48303899 | Rare:81; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48492772-48492859 | Common:1; Rare:17 | ||||
| chr13:48533050-48533371 | Common:2; Rare:87 | ||||
| chr13:48653553-48653802 | Rare:46 | ||||
| chr13:48975836-48975952 | Rare:40 | ||||
| chr13:48976370-48976666 | Common:3; Rare:103 | ||||
| chr13:49110237-49110386 | Common:2; Rare:41 | ||||
| chr13:49247800-49247982 | Rare:51 |