| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43879674-43879740 | Common:2; Rare:10 | ||||
| chr13:43879743-43879932 | Common:15; Rare:55 | ||||
| chr13:44436537-44436879 | Common:2; Rare:94 | ||||
| chr13:44989410-44989641 | Rare:99 | ||||
| chr13:45120377-45120605 | Common:2; Rare:75 | ||||
| chr13:45341040-45341609 | Common:4; Rare:258 | ||||
| chr13:45418336-45418555 | Rare:66 | ||||
| chr13:45464676-45465048 | Common:1; Rare:96 | ||||
| chr13:46052467-46052497 | Rare:7 | ||||
| chr13:46052638-46052867 | Common:2; Rare:57 | ||||
| chr13:46182125-46182451 | Common:3; Rare:56 | ||||
| chr13:46211759-46211992 | Common:2; Rare:71 | ||||
| chr13:46387203-46387395 | Rare:55 | ||||
| chr13:48001237-48001405 | Common:1; Rare:78; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:48037691-48037789 | Common:1; Rare:55 |