| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:24723839-24723891 | Rare:14 | ||||
| chr10:24724123-24724181 | Rare:15 | ||||
| chr10:24952281-24952350 | Rare:10 | ||||
| chr10:24952820-24952971 | Rare:45 | ||||
| chr10:25016430-25016724 | Common:9; Rare:121 | ||||
| chr10:25016935-25017158 | Common:4; Rare:93 | ||||
| chr10:26437656-26437740 | Common:1; Rare:13 | ||||
| chr10:26437746-26437980 | Rare:36 | ||||
| chr10:26437993-26438453 | Common:2; Rare:104 | ||||
| chr10:26438603-26438942 | Common:5; Rare:81 | ||||
| chr10:26697137-26697748 | Common:4; Rare:156; Clinvar (benign):1 | ||||
| chr10:26697816-26698033 | Common:2; Rare:57 | ||||
| chr10:26860440-26860698 | Common:3; Rare:52 | ||||
| chr10:26860740-26861043 | Common:2; Rare:103 | ||||
| chr10:27099982-27100269 | Common:1; Rare:116; Clinvar:5; Clinvar (benign):2 |