| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118548260-118548390 | Common:1; Rare:24; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:118893913-118894241 | Common:3; Rare:98 | ||||
| chr6:118934976-118935106 | Common:4; Rare:47 | ||||
| chr6:119349679-119349936 | Common:3; Rare:87 | ||||
| chr6:124963023-124963308 | Common:1; Rare:94 | ||||
| chr6:125260600-125260856 | Common:4; Rare:50 | ||||
| chr6:125749401-125749760 | Common:5; Rare:142 | ||||
| chr6:125781020-125781201 | Rare:31 | ||||
| chr6:125986433-125986548 | Rare:45 | ||||
| chr6:127266762-127266925 | Common:2; Rare:74 | ||||
| chr6:127343349-127343564 | Common:1; Rare:43 | ||||
| chr6:127343567-127343627 | Common:1; Rare:17 | ||||
| chr6:128520462-128520781 | Common:3; Rare:101 | ||||
| chr6:128883077-128883373 | Common:2; Rare:79; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr6:128883450-128883647 | Common:2; Rare:42 |