| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:123008375-123008426 | Rare:5 | ||||
| chr10:123008734-123009083 | Common:7; Rare:106; Clinvar:5; Clinvar (benign):6 | ||||
| chr10:123154026-123154377 | Common:5; Rare:79 | ||||
| chr10:123154385-123154501 | Common:2; Rare:48 | ||||
| chr10:123154680-123154819 | Rare:33 | ||||
| chr10:124403561-124403779 | Common:1; Rare:54 | ||||
| chr10:124418900-124419128 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:124461679-124461871 | Common:5; Rare:63 | ||||
| chr10:124462018-124462075 | Common:1; Rare:20 | ||||
| chr10:124744366-124744550 | Rare:62 | ||||
| chr10:124791370-124791457 | Common:1; Rare:19 | ||||
| chr10:124791745-124792064 | Common:3; Rare:153 | ||||
| chr10:124792174-124792220 | Rare:11 | ||||
| chr10:124801611-124801900 | Rare:96 | ||||
| chr10:125719379-125719796 | Common:1; Rare:155 |