| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96566820-96567124 | Common:1; Rare:87 | ||||
| chr9:96655293-96655424 | Rare:35 | ||||
| chr9:96778049-96778154 | Rare:33 | ||||
| chr9:97633271-97633875 | Common:6; Rare:189 | ||||
| chr9:97922179-97922280 | Common:1; Rare:31 | ||||
| chr9:97922471-97922591 | Common:3; Rare:57 | ||||
| chr9:97983160-97983448 | Common:1; Rare:112 | ||||
| chr9:97984227-97984589 | Common:1; Rare:153 | ||||
| chr9:98056507-98056783 | Common:1; Rare:91 | ||||
| chr9:98119310-98119574 | Common:1; Rare:48 | ||||
| chr9:98192623-98192818 | Common:5; Rare:55 | ||||
| chr9:98255552-98255854 | Common:3; Rare:92 | ||||
| chr9:98943486-98943959 | Common:5; Rare:131 | ||||
| chr9:99221898-99222333 | Common:2; Rare:170; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99821650-99822000 | Rare:108 |