| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107283121-107283284 | Common:1; Rare:49 | ||||
| chr9:108934065-108934477 | Common:7; Rare:162; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498244-109498455 | Rare:68 | ||||
| chr9:110048521-110048724 | Common:1; Rare:60 | ||||
| chr9:110125320-110125576 | Rare:53 | ||||
| chr9:110256431-110256723 | Common:5; Rare:105 | ||||
| chr9:111661487-111661653 | Common:3; Rare:43 | ||||
| chr9:112379834-112380150 | Common:3; Rare:130 | ||||
| chr9:113221262-113221584 | Rare:102 | ||||
| chr9:113275392-113275689 | Common:4; Rare:85; Clinvar (pathogenic):1 | ||||
| chr9:113410289-113410705 | Common:3; Rare:123 | ||||
| chr9:114587516-114587908 | Common:3; Rare:153 | ||||
| chr9:115118009-115118133 | Common:3; Rare:32 | ||||
| chr9:116687228-116687352 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:120793257-120793527 | Common:1; Rare:97 |