| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:116687243-116687367 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120477479-120477532 | Rare:9 | ||||
| chr9:120793367-120793527 | Rare:60 | ||||
| chr9:120842896-120843112 | Common:1; Rare:81 | ||||
| chr9:121201857-121202141 | Common:2; Rare:78 | ||||
| chr9:121370231-121370524 | Common:1; Rare:78 | ||||
| chr9:122264776-122264919 | Common:2; Rare:43 | ||||
| chr9:122931457-122931694 | Common:3; Rare:52 | ||||
| chr9:124940966-124941181 | Common:3; Rare:74 | ||||
| chr9:125189721-125189735 | Rare:3 | ||||
| chr9:125189753-125190029 | Common:1; Rare:111 | ||||
| chr9:125261713-125261851 | Common:1; Rare:48 | ||||
| chr9:127122711-127123007 | Common:3; Rare:86 | ||||
| chr9:127451375-127451519 | Common:1; Rare:49 | ||||
| chr9:127854301-127854383 | Common:1; Rare:20; Clinvar:1; Clinvar (benign):2 |