| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:23095346-23095637 | Rare:56 | ||||
| chr10:23438734-23439023 | Common:4; Rare:97 | ||||
| chr10:23439167-23439297 | Common:2; Rare:37 | ||||
| chr10:24466386-24466582 | Rare:34 | ||||
| chr10:24722813-24722914 | Common:1; Rare:29 | ||||
| chr10:24722933-24723098 | Common:1; Rare:38 | ||||
| chr10:24723866-24724047 | Common:3; Rare:40 | ||||
| chr10:25016423-25016719 | Common:9; Rare:119 | ||||
| chr10:25016960-25017129 | Common:4; Rare:77 | ||||
| chr10:25061680-25062080 | Common:5; Rare:96 | ||||
| chr10:25465897-25466245 | Common:2; Rare:76 | ||||
| chr10:26697540-26697712 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr10:26697780-26698060 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:26860772-26861356 | Common:7; Rare:163 | ||||
| chr10:27100394-27100667 | Common:4; Rare:73; Clinvar:4; Clinvar (benign):2 |