| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:110892151-110892420 | Rare:65 | ||||
| chr6:110958590-110958806 | Common:5; Rare:89 | ||||
| chr6:110981861-110982114 | Common:3; Rare:112 | ||||
| chr6:111605835-111606138 | Common:2; Rare:51 | ||||
| chr6:112087277-112087686 | Common:1; Rare:145 | ||||
| chr6:116060737-116060961 | Common:1; Rare:46 | ||||
| chr6:116100651-116100913 | Common:1; Rare:105 | ||||
| chr6:116254068-116254242 | Common:4; Rare:44 | ||||
| chr6:116278753-116279004 | Rare:73 | ||||
| chr6:116279528-116279776 | Common:2; Rare:82 | ||||
| chr6:116279841-116280108 | Common:2; Rare:91 | ||||
| chr6:116571202-116571618 | Common:3; Rare:119 | ||||
| chr6:117573520-117573849 | Common:1; Rare:63 | ||||
| chr6:117602417-117602660 | Common:4; Rare:65 | ||||
| chr6:118548035-118548328 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 |