| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127794430-127794649 | Rare:53 | ||||
| chr9:127802691-127803047 | Common:3; Rare:98 | ||||
| chr9:127803144-127803353 | Common:1; Rare:49 | ||||
| chr9:127809826-127810059 | Common:3; Rare:78 | ||||
| chr9:127854610-127854877 | Rare:55; Clinvar:5 | ||||
| chr9:127897321-127897546 | Common:1; Rare:49 | ||||
| chr9:127898458-127898575 | Common:1; Rare:18 | ||||
| chr9:127937811-127937923 | Common:1; Rare:32; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128098262-128098574 | Common:1; Rare:69 | ||||
| chr9:128103078-128103362 | Common:1; Rare:53 | ||||
| chr9:128190385-128190593 | Rare:53 | ||||
| chr9:128191750-128191827 | Common:1; Rare:19 | ||||
| chr9:128275919-128276324 | Common:5; Rare:184 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322729-128322887 | Common:2; Rare:72; Clinvar (benign):5 |