| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130372596-130372702 | Rare:38 | ||||
| chr2:131093382-131093569 | Common:1; Rare:87 | ||||
| chr2:131105193-131105375 | Common:1; Rare:84 | ||||
| chr2:131492762-131493107 | Common:8; Rare:106 | ||||
| chr2:134918580-134918863 | Common:1; Rare:111 | ||||
| chr2:135052216-135052311 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr2:135531172-135531521 | Common:1; Rare:74 | ||||
| chr2:135741716-135741956 | Common:1; Rare:92 | ||||
| chr2:135985381-135985685 | Common:4; Rare:131; Clinvar (benign):1 | ||||
| chr2:136118142-136118310 | Rare:45 | ||||
| chr2:138501664-138502077 | Common:2; Rare:140 | ||||
| chr2:144518134-144518280 | Common:2; Rare:38 | ||||
| chr2:144520099-144520561 | Common:4; Rare:79; Clinvar (benign):1 | ||||
| chr2:148020681-148021109 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:148021331-148021477 | Rare:30 |