| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99559418-99559786 | Rare:56 | ||||
| chr13:100262569-100262794 | Rare:63; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr13:100540272-100540531 | Common:2; Rare:42 | ||||
| chr13:102853925-102854331 | Common:1; Rare:80; Clinvar (pathogenic):1 | ||||
| chr13:105919224-105919376 | Common:2; Rare:31 | ||||
| chr13:105929589-105929854 | Common:2; Rare:49 | ||||
| chr13:105979283-105979455 | Rare:35 | ||||
| chr13:106151350-106151638 | Common:1; Rare:59 | ||||
| chr13:106472771-106472911 | Common:1; Rare:24 | ||||
| chr13:106512404-106512688 | Rare:38 | ||||
| chr13:106512785-106512840 | Rare:18 | ||||
| chr13:106522065-106522120 | Common:1; Rare:17 | ||||
| chr13:108510447-108510454 | Common:1; Rare:1 | ||||
| chr13:109147318-109147598 | Common:3; Rare:63 | ||||
| chr13:109148297-109148550 | Common:1; Rare:47 |