| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:2903243-2903466 | Common:5; Rare:59 | ||||
| chr6:2971266-2971717 | Common:5; Rare:116 | ||||
| chr6:2999632-3000085 | Common:11; Rare:100 | ||||
| chr6:3063788-3063968 | Common:1; Rare:70 | ||||
| chr6:3068275-3068596 | Common:1; Rare:105 | ||||
| chr6:3118602-3118750 | Common:2; Rare:50 | ||||
| chr6:3157526-3157642 | Common:6; Rare:46 | ||||
| chr6:3456020-3456175 | Rare:49 | ||||
| chr6:3751951-3752293 | Common:5; Rare:113 | ||||
| chr6:3849130-3849465 | Common:3; Rare:95 | ||||
| chr6:4021187-4021460 | Rare:118 | ||||
| chr6:5003649-5003843 | Common:5; Rare:61 | ||||
| chr6:5004007-5004126 | Common:1; Rare:53 | ||||
| chr6:5132739-5132973 | Common:2; Rare:48 | ||||
| chr6:5260671-5261060 | Common:6; Rare:141; Clinvar (benign):4 |