| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89638712-89638837 | Common:3; Rare:46 | ||||
| chr6:89819688-89819926 | Rare:78 | ||||
| chr6:89829614-89829955 | Rare:89 | ||||
| chr6:90586984-90587266 | Common:3; Rare:79 | ||||
| chr6:93419552-93419831 | Common:1; Rare:74 | ||||
| chr6:95577408-95577553 | Common:3; Rare:40 | ||||
| chr6:96521622-96521887 | Common:9; Rare:127 | ||||
| chr6:96897764-96898012 | Common:2; Rare:96; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:97283135-97283314 | Common:1; Rare:55 | ||||
| chr6:99424793-99424933 | Rare:44 | ||||
| chr6:99425214-99425506 | Common:2; Rare:86 | ||||
| chr6:99515400-99515613 | Common:1; Rare:68 | ||||
| chr6:100881189-100881483 | Common:6; Rare:106 | ||||
| chr6:104957010-104957099 | Rare:14 | ||||
| chr6:106325403-106325510 | Common:1; Rare:22 |