| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906575-99906690 | Rare:60 | ||||
| chr9:100098979-100099314 | Common:2; Rare:92; Clinvar:2 | ||||
| chr9:100352853-100353094 | Rare:89 | ||||
| chr9:101398580-101398910 | Common:1; Rare:108 | ||||
| chr9:101533728-101533894 | Rare:50 | ||||
| chr9:104093985-104094350 | Common:3; Rare:89 | ||||
| chr9:104747608-104747731 | Rare:30 | ||||
| chr9:105558067-105558153 | Rare:23 | ||||
| chr9:105694381-105694623 | Common:4; Rare:101 | ||||
| chr9:107282962-107283284 | Common:2; Rare:111 | ||||
| chr9:108934063-108934477 | Common:7; Rare:162; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:110148506-110148663 | Common:1; Rare:34 | ||||
| chr9:110256440-110256725 | Common:5; Rare:103 | ||||
| chr9:111661490-111661653 | Common:3; Rare:42 | ||||
| chr9:112333571-112333949 | Rare:120 |