| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:100881249-100881498 | Common:5; Rare:97 | ||||
| chr6:105137121-105137272 | Common:1; Rare:60 | ||||
| chr6:105179907-105180139 | Common:6; Rare:60 | ||||
| chr6:106325586-106325892 | Common:1; Rare:108 | ||||
| chr6:106629448-106629588 | Common:1; Rare:29 | ||||
| chr6:109382385-109382829 | Common:6; Rare:145; Clinvar (benign):1 | ||||
| chr6:109691159-109691315 | Common:1; Rare:38; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:110874678-110874789 | Common:3; Rare:37 | ||||
| chr6:110958600-110958788 | Common:5; Rare:69 | ||||
| chr6:110981857-110982109 | Common:3; Rare:112 | ||||
| chr6:112087446-112087678 | Rare:71 | ||||
| chr6:113971100-113971427 | Common:3; Rare:103 | ||||
| chr6:116254073-116254222 | Common:4; Rare:39 | ||||
| chr6:116571175-116571580 | Common:3; Rare:118 | ||||
| chr6:117602466-117602641 | Common:3; Rare:51 |