| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:24721219-24721995 | Rare:342 | ||||
| chr10:24722109-24722614 | Common:3; Rare:230 | ||||
| chr10:24722560-24723260 | Common:9; Rare:608 | ||||
| chr10:24723170-24724510 | Common:21; Rare:689 | ||||
| chr10:24951936-24953739 | Common:32; Rare:1569 | ||||
| chr10:25015970-25016764 | Common:33; Rare:532 | ||||
| chr10:25016841-25017241 | Common:30; Rare:677 | ||||
| chr10:25061142-25061868 | Common:2; Rare:140 | ||||
| chr10:25061799-25061949 | Common:2; Rare:27 | ||||
| chr10:25061859-25062320 | Common:6; Rare:155 | ||||
| chr10:25062430-25062960 | Common:10; Rare:155 | ||||
| chr10:25465749-25466383 | Common:12; Rare:355 | ||||
| chr10:26696770-26697240 | Common:3; Rare:98 | ||||
| chr10:26697200-26697490 | Common:10; Rare:148 | ||||
| chr10:26697544-26698090 | Common:13; Rare:530; Clinvar:6; Clinvar (benign):11 |