| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100352831-100353089 | Rare:93 | ||||
| chr9:101398505-101398998 | Common:1; Rare:160 | ||||
| chr9:101487028-101487248 | Common:3; Rare:57 | ||||
| chr9:101533720-101533914 | Rare:60 | ||||
| chr9:104093737-104093781 | Common:3; Rare:12 | ||||
| chr9:104093985-104094350 | Common:3; Rare:89 | ||||
| chr9:104747601-104747799 | Common:1; Rare:61 | ||||
| chr9:104747840-104747979 | Common:3; Rare:55 | ||||
| chr9:104763972-104764243 | Common:2; Rare:60 | ||||
| chr9:104764270-104764356 | Common:1; Rare:36 | ||||
| chr9:104928037-104928402 | Common:6; Rare:87; Clinvar:2; Clinvar (benign):4 | ||||
| chr9:105447976-105448153 | Common:2; Rare:65 | ||||
| chr9:105558033-105558175 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862964-106863186 | Rare:76 | ||||
| chr9:106863536-106863660 | Rare:22 |