| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:18659749-18660008 | Common:3; Rare:70 | ||||
| chr10:19816430-19816451 | Rare:1 | ||||
| chr10:23439275-23439464 | Common:1; Rare:62 | ||||
| chr10:26438035-26438412 | Common:2; Rare:86 | ||||
| chr10:27154185-27154493 | Rare:87 | ||||
| chr10:27155146-27155279 | Common:1; Rare:45; Clinvar:5; Clinvar (benign):1 | ||||
| chr10:27240514-27240640 | Common:2; Rare:40 | ||||
| chr10:28532620-28532836 | Common:1; Rare:93 | ||||
| chr10:28533026-28533194 | Rare:66 | ||||
| chr10:28533202-28533520 | Common:1; Rare:115 | ||||
| chr10:29735794-29736029 | Common:3; Rare:48 | ||||
| chr10:30433836-30434239 | Common:4; Rare:125 | ||||
| chr10:31031841-31032031 | Common:1; Rare:73 | ||||
| chr10:31928797-31928950 | Common:1; Rare:59 | ||||
| chr10:32378723-32378900 | Common:1; Rare:24 |