| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101533709-101533905 | Rare:62 | ||||
| chr9:104094029-104094345 | Common:2; Rare:66 | ||||
| chr9:104094431-104094603 | Common:2; Rare:46 | ||||
| chr9:104747612-104747767 | Rare:44 | ||||
| chr9:105558062-105558159 | Rare:30; Clinvar (benign):1 | ||||
| chr9:108934052-108934502 | Common:7; Rare:179; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109013447-109013760 | Common:2; Rare:109 | ||||
| chr9:112379838-112380150 | Common:3; Rare:128 | ||||
| chr9:113056657-113056848 | Common:1; Rare:67; Clinvar:1 | ||||
| chr9:113187994-113188143 | Common:2; Rare:22 | ||||
| chr9:113221262-113221628 | Rare:114 | ||||
| chr9:113275368-113275734 | Common:5; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:114587612-114587881 | Common:1; Rare:98 | ||||
| chr9:116687228-116687364 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580103-120580403 | Common:1; Rare:93; Clinvar:5 |