| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113275363-113275746 | Common:5; Rare:122; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340430 | Common:3; Rare:48 | ||||
| chr9:113376868-113377138 | Common:9; Rare:83 | ||||
| chr9:113401214-113401579 | Common:6; Rare:127; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410197-113410760 | Common:4; Rare:183 | ||||
| chr9:113565347-113565607 | Common:1; Rare:61 | ||||
| chr9:113580713-113580955 | Common:3; Rare:42 | ||||
| chr9:114387967-114388119 | Common:1; Rare:50 | ||||
| chr9:114505394-114505704 | Common:3; Rare:91; Clinvar (benign):1 | ||||
| chr9:114587598-114587910 | Common:2; Rare:115 | ||||
| chr9:116687203-116687364 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:117704174-117704478 | Common:2; Rare:66 | ||||
| chr9:120714452-120714754 | Common:2; Rare:103 | ||||
| chr9:120793192-120793540 | Common:2; Rare:123 | ||||
| chr9:120842897-120843278 | Common:1; Rare:125 |