| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144901400-144901708 | Common:1; Rare:88 | ||||
| chr9:504391-504742 | Common:4; Rare:169 | ||||
| chr9:2621860-2622198 | Common:6; Rare:118; Clinvar:8; Clinvar (benign):3 | ||||
| chr9:2844043-2844331 | Common:5; Rare:106 | ||||
| chr9:3526409-3526494 | Common:4; Rare:42 | ||||
| chr9:4679437-4679781 | Common:1; Rare:150 | ||||
| chr9:4741038-4741377 | Common:4; Rare:163 | ||||
| chr9:5450420-5450596 | Common:5; Rare:68 | ||||
| chr9:5628979-5629235 | Common:1; Rare:115 | ||||
| chr9:6757865-6758087 | Common:5; Rare:83 | ||||
| chr9:13279502-13279811 | Common:4; Rare:92 | ||||
| chr9:14313483-14313547 | Rare:18 | ||||
| chr9:14693265-14693355 | Common:1; Rare:45 | ||||
| chr9:15472673-15472995 | Rare:81 | ||||
| chr9:19049337-19049436 | Rare:43 |