| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113221262-113221607 | Rare:108 | ||||
| chr9:113275392-113275745 | Common:5; Rare:119; Clinvar (pathogenic):1 | ||||
| chr9:113410281-113410723 | Common:3; Rare:131 | ||||
| chr9:114587600-114587856 | Common:2; Rare:94 | ||||
| chr9:115118061-115118141 | Common:2; Rare:24 | ||||
| chr9:115118151-115118459 | Rare:70 | ||||
| chr9:116687240-116687364 | Common:1; Rare:40; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793254-120793543 | Common:2; Rare:108 | ||||
| chr9:120842906-120843107 | Common:1; Rare:71 | ||||
| chr9:120877147-120877482 | Common:3; Rare:109 | ||||
| chr9:121074860-121074967 | Rare:50 | ||||
| chr9:121201838-121202149 | Common:2; Rare:89 | ||||
| chr9:122264737-122264922 | Common:2; Rare:53 | ||||
| chr9:122913309-122913426 | Common:2; Rare:29 | ||||
| chr9:122931488-122931668 | Common:3; Rare:34 |