| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:186783143-186783608 | Common:2; Rare:188 | ||||
| chr3:186783973-186784373 | Common:5; Rare:231 | ||||
| chr3:186806389-186806622 | Rare:76 | ||||
| chr3:186806715-186807115 | Common:6; Rare:114 | ||||
| chr3:186930080-186930680 | Common:5; Rare:130 | ||||
| chr3:187139395-187139604 | Common:1; Rare:81 | ||||
| chr3:187291579-187292101 | Common:27; Rare:450 | ||||
| chr3:187737505-187738170 | Common:4; Rare:130 | ||||
| chr3:188153763-188153986 | Common:1; Rare:40 | ||||
| chr3:188154371-188154555 | Common:1; Rare:50 | ||||
| chr3:188947662-188947822 | Common:1; Rare:57 | ||||
| chr3:190120810-190121140 | Rare:91 | ||||
| chr3:190513856-190514109 | Common:2; Rare:74 | ||||
| chr3:190514260-190514730 | Common:1; Rare:93 | ||||
| chr3:191329559-191329869 | Common:3; Rare:99; Clinvar (benign):1 |