| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106495404-106495604 | Common:5; Rare:30 | ||||
| chr6:106510779-106510907 | Common:3; Rare:29 | ||||
| chr6:106526973-106527052 | Rare:9 | ||||
| chr6:106530050-106530318 | Common:1; Rare:69 | ||||
| chr6:106539114-106539441 | Common:4; Rare:64 | ||||
| chr6:106715988-106716083 | Rare:14 | ||||
| chr6:106739517-106739779 | Common:2; Rare:47 | ||||
| chr6:106746711-106746995 | Common:1; Rare:56 | ||||
| chr6:106747355-106747452 | Common:1; Rare:11 | ||||
| chr6:106872233-106872357 | Common:1; Rare:24 | ||||
| chr6:106972729-106972998 | Common:1; Rare:37 | ||||
| chr6:106973295-106973502 | Rare:46 | ||||
| chr6:107184929-107185158 | Rare:36 | ||||
| chr6:107375755-107375994 | Common:4; Rare:34 | ||||
| chr6:107876562-107876856 | Common:6; Rare:86; Clinvar (benign):1 |