| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113376901-113377055 | Common:7; Rare:54 | ||||
| chr9:113401233-113401529 | Common:6; Rare:110; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410175-113410826 | Common:4; Rare:215 | ||||
| chr9:113463581-113463778 | Common:1; Rare:68 | ||||
| chr9:113564944-113565155 | Rare:44 | ||||
| chr9:113593867-113594168 | Common:4; Rare:118 | ||||
| chr9:114387964-114388103 | Common:1; Rare:47 | ||||
| chr9:114505368-114505705 | Common:3; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:114587602-114587967 | Common:3; Rare:139 | ||||
| chr9:115112787-115112898 | Common:1; Rare:20 | ||||
| chr9:116687203-116687372 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:119369422-119369467 | Rare:9 | ||||
| chr9:119369472-119369754 | Rare:65 | ||||
| chr9:120579907-120580315 | Common:2; Rare:145; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:120793077-120793575 | Common:7; Rare:165 |