| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:100969438-100969566 | Common:1; Rare:25 | ||||
| chr10:100987286-100987607 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:100996468-100996587 | Rare:23 | ||||
| chr10:100996940-100997293 | Common:2; Rare:90 | ||||
| chr10:100997519-100997679 | Common:1; Rare:37 | ||||
| chr10:100997748-100997969 | Common:1; Rare:42 | ||||
| chr10:100998487-100998810 | Common:3; Rare:53 | ||||
| chr10:100999193-100999507 | Common:3; Rare:60 | ||||
| chr10:100999637-100999829 | Common:1; Rare:55 | ||||
| chr10:101019032-101019193 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:101031079-101031503 | Common:1; Rare:99 | ||||
| chr10:101061604-101062002 | Rare:65 | ||||
| chr10:101066011-101066587 | Common:1; Rare:155 | ||||
| chr10:101066643-101066815 | Common:2; Rare:36 | ||||
| chr10:101353871-101354210 | Common:1; Rare:112 |