| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:29736559-29736609 | Common:1; Rare:5 | ||||
| chr10:29736887-29737151 | Common:2; Rare:79 | ||||
| chr10:30059494-30059606 | Common:1; Rare:45 | ||||
| chr10:30348839-30349114 | Common:2; Rare:72; Clinvar (benign):1 | ||||
| chr10:30349207-30349463 | Common:12; Rare:107 | ||||
| chr10:30433349-30433643 | Common:1; Rare:81 | ||||
| chr10:30433673-30434287 | Common:4; Rare:173 | ||||
| chr10:30434437-30434742 | Common:2; Rare:78 | ||||
| chr10:30434781-30434848 | Rare:11 | ||||
| chr10:31031561-31031734 | Common:2; Rare:39 | ||||
| chr10:31031759-31032091 | Common:2; Rare:136 | ||||
| chr10:31032320-31032611 | Common:13; Rare:92 | ||||
| chr10:31928272-31928630 | Common:4; Rare:110 | ||||
| chr10:31928643-31929020 | Common:4; Rare:126 | ||||
| chr10:31929337-31929567 | Common:3; Rare:46 |