| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39655575-39655769 | Common:4; Rare:104; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:40771138-40771353 | Common:3; Rare:71 | ||||
| chr13:40789370-40789609 | Common:2; Rare:79; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:40792758-40792895 | Rare:20 | ||||
| chr13:40982856-40983032 | Common:3; Rare:27 | ||||
| chr13:41019273-41019447 | Rare:26 | ||||
| chr13:41060897-41061038 | Common:16; Rare:85 | ||||
| chr13:41061191-41061566 | Common:3; Rare:133 | ||||
| chr13:41194524-41194659 | Common:2; Rare:33 | ||||
| chr13:41311189-41311298 | Rare:47 | ||||
| chr13:41457434-41457551 | Common:2; Rare:39 | ||||
| chr13:41463969-41464122 | Rare:23 | ||||
| chr13:42271838-42272145 | Common:3; Rare:80 | ||||
| chr13:43023512-43023633 | Common:1; Rare:45 | ||||
| chr13:43879716-43879862 | Common:18; Rare:50 |