| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109009414-109009689 | Common:2; Rare:84 | ||||
| chr6:109094205-109094607 | Rare:88 | ||||
| chr6:109094856-109095197 | Common:5; Rare:105 | ||||
| chr6:109095407-109095557 | Rare:33 | ||||
| chr6:109381737-109381756 | Rare:6 | ||||
| chr6:109382051-109382860 | Common:11; Rare:290; Clinvar (benign):2 | ||||
| chr6:109440514-109441011 | Common:2; Rare:163 | ||||
| chr6:109455696-109456074 | Common:3; Rare:97 | ||||
| chr6:109483117-109483236 | Rare:57 | ||||
| chr6:109691151-109691339 | Common:3; Rare:45; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179962-110180167 | Common:2; Rare:61 | ||||
| chr6:110415532-110415644 | Rare:26 | ||||
| chr6:110814374-110814633 | Common:1; Rare:84 | ||||
| chr6:110875403-110875451 | Rare:9 | ||||
| chr6:110958592-110958788 | Common:5; Rare:73 |