| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37869739-37869940 | Common:1; Rare:50 | ||||
| chr13:37870300-37870616 | Common:2; Rare:63 | ||||
| chr13:38349421-38349914 | Common:5; Rare:155; Clinvar (pathogenic):1 | ||||
| chr13:38349945-38349998 | Common:1; Rare:24 | ||||
| chr13:38350194-38350317 | Rare:53 | ||||
| chr13:38686853-38687127 | Common:3; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:38821927-38822046 | Common:2; Rare:18 | ||||
| chr13:39037747-39038402 | Common:2; Rare:185 | ||||
| chr13:39038699-39038761 | Rare:17 | ||||
| chr13:39602660-39602761 | Rare:28 | ||||
| chr13:39603096-39603477 | Common:2; Rare:132 | ||||
| chr13:39603523-39603794 | Common:2; Rare:45 | ||||
| chr13:39655565-39655763 | Common:4; Rare:107; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40666547-40666918 | Common:3; Rare:125 | ||||
| chr13:40770851-40770979 | Common:1; Rare:33 |