| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:105558079-105558189 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862973-106863180 | Rare:72 | ||||
| chr9:107488423-107488577 | Common:1; Rare:47 | ||||
| chr9:108933945-108934493 | Common:8; Rare:217; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:109498227-109498464 | Rare:74 | ||||
| chr9:110125314-110125553 | Rare:53 | ||||
| chr9:111525065-111525231 | Common:3; Rare:54 | ||||
| chr9:112379798-112380146 | Common:3; Rare:140 | ||||
| chr9:112718002-112718327 | Common:2; Rare:76 | ||||
| chr9:113188007-113188176 | Common:2; Rare:21 | ||||
| chr9:113221235-113221640 | Common:1; Rare:129 | ||||
| chr9:113275376-113275734 | Common:5; Rare:114; Clinvar (pathogenic):1 | ||||
| chr9:113340246-113340431 | Common:3; Rare:46 | ||||
| chr9:113401263-113401556 | Common:6; Rare:107; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410281-113410734 | Common:3; Rare:138 |