| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:111661487-111661703 | Common:3; Rare:61 | ||||
| chr9:112379800-112380179 | Common:3; Rare:146 | ||||
| chr9:112718008-112718160 | Common:2; Rare:36 | ||||
| chr9:113056657-113056836 | Common:1; Rare:64; Clinvar:1 | ||||
| chr9:113188022-113188189 | Common:2; Rare:19 | ||||
| chr9:113221235-113221610 | Common:1; Rare:120 | ||||
| chr9:113275354-113275745 | Common:5; Rare:128; Clinvar (pathogenic):1 | ||||
| chr9:113376877-113377096 | Common:8; Rare:68 | ||||
| chr9:113401218-113401545 | Common:6; Rare:120; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410219-113410687 | Common:2; Rare:137 | ||||
| chr9:114387980-114388176 | Common:1; Rare:55 | ||||
| chr9:115117985-115118434 | Common:3; Rare:109 | ||||
| chr9:116687207-116687364 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120793227-120793534 | Common:1; Rare:110 | ||||
| chr9:120842904-120843280 | Common:1; Rare:121 |