| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:24951809-24952200 | Common:2; Rare:62 | ||||
| chr10:24952281-24952405 | Rare:30 | ||||
| chr10:24952528-24952620 | Common:2; Rare:35 | ||||
| chr10:24952714-24953220 | Common:2; Rare:124 | ||||
| chr10:25016031-25016268 | Common:2; Rare:59 | ||||
| chr10:25016411-25016748 | Common:10; Rare:136 | ||||
| chr10:25016878-25017159 | Common:6; Rare:115 | ||||
| chr10:25062167-25062218 | Rare:9 | ||||
| chr10:25062252-25062738 | Common:2; Rare:83 | ||||
| chr10:26697078-26697298 | Rare:43 | ||||
| chr10:26697301-26697465 | Common:3; Rare:40 | ||||
| chr10:26697527-26698021 | Common:4; Rare:145; Clinvar:2; Clinvar (benign):3 | ||||
| chr10:26734198-26734286 | Rare:18 | ||||
| chr10:26734295-26734488 | Common:2; Rare:29 | ||||
| chr10:26860128-26860380 | Rare:62 |