| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:117966034-117966143 | Common:1; Rare:44 | ||||
| chr6:118467352-118467461 | Rare:15 | ||||
| chr6:118580793-118581050 | Common:1; Rare:54 | ||||
| chr6:118895097-118895263 | Rare:48 | ||||
| chr6:119016270-119016278 | Rare:2 | ||||
| chr6:119043066-119043266 | Common:4; Rare:38 | ||||
| chr6:119043379-119043533 | Rare:15 | ||||
| chr6:119201640-119201759 | Rare:17 | ||||
| chr6:119202608-119202749 | Common:3; Rare:18 | ||||
| chr6:119441841-119442015 | Rare:31 | ||||
| chr6:120837334-120837464 | Common:1; Rare:27 | ||||
| chr6:121039957-121040040 | Rare:28 | ||||
| chr6:121437516-121437573 | Common:1; Rare:13 | ||||
| chr6:121686583-121686824 | Common:5; Rare:80 | ||||
| chr6:123571021-123571237 | Common:2; Rare:65; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):1 |