| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113401242-113401502 | Common:6; Rare:98; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410289-113410790 | Common:4; Rare:162 | ||||
| chr9:114587554-114587920 | Common:3; Rare:146 | ||||
| chr9:114611220-114611546 | Common:2; Rare:98 | ||||
| chr9:115118007-115118284 | Common:3; Rare:64 | ||||
| chr9:116687185-116687364 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120579880-120580360 | Common:3; Rare:180; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:120793248-120793551 | Common:2; Rare:112 | ||||
| chr9:120842905-120843139 | Common:1; Rare:85 | ||||
| chr9:120868831-120869107 | Common:2; Rare:57 | ||||
| chr9:120877114-120877518 | Common:3; Rare:133 | ||||
| chr9:121074837-121074969 | Rare:62 | ||||
| chr9:121121678-121121870 | Rare:52 | ||||
| chr9:121201824-121202187 | Common:2; Rare:107 | ||||
| chr9:121268040-121268207 | Common:1; Rare:58 |