| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73096773-73097018 | Common:3; Rare:76 | ||||
| chr10:73097080-73097143 | Common:1; Rare:11 | ||||
| chr10:73167965-73168141 | Rare:42 | ||||
| chr10:73252554-73252802 | Common:2; Rare:71; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:73358718-73358886 | Common:2; Rare:44 | ||||
| chr10:73414010-73414157 | Common:2; Rare:43 | ||||
| chr10:73495610-73495764 | Rare:30 | ||||
| chr10:73625955-73626100 | Rare:25 | ||||
| chr10:73744243-73744430 | Common:1; Rare:50 | ||||
| chr10:73781951-73782091 | Common:1; Rare:47 | ||||
| chr10:73997856-73998169 | Common:1; Rare:89 | ||||
| chr10:74151063-74151267 | Common:1; Rare:62 | ||||
| chr10:74176609-74176778 | Rare:46; Clinvar:2 | ||||
| chr10:74825312-74825517 | Rare:53 | ||||
| chr10:75111530-75111698 | Rare:54 |