| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101533709-101533903 | Rare:61 | ||||
| chr9:104093985-104094350 | Common:3; Rare:89 | ||||
| chr9:104094481-104094603 | Common:2; Rare:39 | ||||
| chr9:104747609-104747788 | Common:1; Rare:55 | ||||
| chr9:105558067-105558170 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862979-106863180 | Rare:69 | ||||
| chr9:106863386-106863660 | Common:1; Rare:51 | ||||
| chr9:107283044-107283289 | Common:1; Rare:82 | ||||
| chr9:108933931-108933995 | Common:2; Rare:24; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:108934074-108934528 | Common:8; Rare:182; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498235-109498379 | Rare:46 | ||||
| chr9:110207512-110207613 | Rare:40 | ||||
| chr9:110208142-110208335 | Common:1; Rare:42 | ||||
| chr9:110256431-110256789 | Common:5; Rare:122 | ||||
| chr9:111525067-111525237 | Common:5; Rare:55 |