| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100298536-100298808 | Common:13; Rare:44 | ||||
| chr13:100299521-100299834 | Common:2; Rare:65 | ||||
| chr13:100300828-100300935 | Rare:22 | ||||
| chr13:100301478-100301623 | Rare:51; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr13:100306496-100306795 | Common:1; Rare:55 | ||||
| chr13:100392738-100393047 | Common:2; Rare:55 | ||||
| chr13:100393051-100393234 | Common:2; Rare:31 | ||||
| chr13:100394136-100394170 | Rare:6 | ||||
| chr13:100514022-100514172 | Rare:29 | ||||
| chr13:100517268-100517430 | Rare:34 | ||||
| chr13:100521306-100521417 | Common:2; Rare:34 | ||||
| chr13:100521453-100521636 | Rare:43 | ||||
| chr13:100521753-100521847 | Rare:22 | ||||
| chr13:100521899-100522153 | Common:1; Rare:47 | ||||
| chr13:100542852-100543104 | Rare:54 |