| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342127-130342281 | Rare:60 | ||||
| chr2:130342645-130342935 | Common:5; Rare:91 | ||||
| chr2:131093382-131093559 | Common:1; Rare:83 | ||||
| chr2:131105192-131105367 | Common:1; Rare:79 | ||||
| chr2:131492091-131492219 | Common:2; Rare:39 | ||||
| chr2:131492276-131492449 | Common:3; Rare:71 | ||||
| chr2:131492762-131493139 | Common:8; Rare:115 | ||||
| chr2:134918571-134918879 | Common:1; Rare:128 | ||||
| chr2:135052167-135052304 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr2:135052627-135052757 | Rare:25 | ||||
| chr2:135530699-135530934 | Common:3; Rare:51 | ||||
| chr2:135531167-135531505 | Common:1; Rare:70 | ||||
| chr2:135741611-135741945 | Common:4; Rare:121 | ||||
| chr2:135876352-135876650 | Common:1; Rare:84 | ||||
| chr2:135984881-135985200 | Common:1; Rare:73 |