| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112379834-112380150 | Common:3; Rare:130 | ||||
| chr9:113056611-113056913 | Common:1; Rare:100; Clinvar:1 | ||||
| chr9:113221230-113221603 | Common:1; Rare:120 | ||||
| chr9:113275359-113275708 | Common:5; Rare:105; Clinvar (pathogenic):1 | ||||
| chr9:113303061-113303208 | Common:1; Rare:28 | ||||
| chr9:113340237-113340431 | Common:3; Rare:49 | ||||
| chr9:113410298-113410569 | Common:1; Rare:88 | ||||
| chr9:113463606-113463769 | Common:1; Rare:56 | ||||
| chr9:114098420-114098533 | Common:5; Rare:27 | ||||
| chr9:114099257-114099413 | Common:1; Rare:33 | ||||
| chr9:114387983-114388166 | Common:1; Rare:52 | ||||
| chr9:114505474-114505622 | Common:1; Rare:43 | ||||
| chr9:114587411-114587910 | Common:4; Rare:173 | ||||
| chr9:115118149-115118456 | Rare:71 | ||||
| chr9:116687228-116687364 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):1 |