| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:121378578-121378642 | Rare:13 | ||||
| chr10:121418418-121418488 | Rare:16 | ||||
| chr10:121426420-121426652 | Common:3; Rare:40 | ||||
| chr10:121428738-121429039 | Common:2; Rare:58 | ||||
| chr10:121434046-121434220 | Common:1; Rare:30 | ||||
| chr10:121435538-121435714 | Common:3; Rare:31 | ||||
| chr10:121436596-121436716 | Common:1; Rare:19 | ||||
| chr10:121449121-121449368 | Common:1; Rare:38 | ||||
| chr10:121455466-121455763 | Common:4; Rare:74 | ||||
| chr10:121495727-121496035 | Common:2; Rare:63 | ||||
| chr10:121500614-121500895 | Rare:79; Clinvar (benign):2 | ||||
| chr10:121512008-121512309 | Common:2; Rare:53 | ||||
| chr10:121513637-121513765 | Rare:17 | ||||
| chr10:121553923-121554122 | Common:1; Rare:39 | ||||
| chr10:121580659-121580887 | Common:4; Rare:41 |