| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:96897803-96898086 | Common:4; Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283089-97283318 | Common:2; Rare:65 | ||||
| chr6:99424828-99424971 | Rare:54 | ||||
| chr6:99425242-99425494 | Common:2; Rare:70 | ||||
| chr6:99515382-99515577 | Common:1; Rare:68 | ||||
| chr6:100881167-100881506 | Common:6; Rare:123 | ||||
| chr6:104859800-104859983 | Rare:61 | ||||
| chr6:104957016-104957153 | Rare:23 | ||||
| chr6:105137059-105137317 | Common:2; Rare:91 | ||||
| chr6:105179856-105180081 | Common:4; Rare:61 | ||||
| chr6:106325551-106325906 | Common:1; Rare:118 | ||||
| chr6:106629432-106629658 | Common:4; Rare:56 | ||||
| chr6:107459534-107459628 | Common:1; Rare:24 | ||||
| chr6:107958075-107958408 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074666-108074871 | Common:1; Rare:70; Clinvar:1 |