| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130836735-130836928 | Common:2; Rare:72 | ||||
| chr2:131093343-131093582 | Common:1; Rare:106 | ||||
| chr2:131105262-131105384 | Common:2; Rare:62 | ||||
| chr2:131492292-131492502 | Common:6; Rare:95 | ||||
| chr2:131492754-131493097 | Common:8; Rare:103 | ||||
| chr2:134918215-134918296 | Common:1; Rare:24 | ||||
| chr2:134918585-134918863 | Common:1; Rare:110 | ||||
| chr2:135052217-135052304 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr2:135530710-135530987 | Common:3; Rare:65 | ||||
| chr2:135531177-135531514 | Common:1; Rare:70 | ||||
| chr2:135741611-135741951 | Common:4; Rare:122 | ||||
| chr2:135876400-135876633 | Rare:63 | ||||
| chr2:135985404-135985694 | Common:4; Rare:126; Clinvar (benign):1 | ||||
| chr2:136118142-136118319 | Rare:46 | ||||
| chr2:138501645-138502022 | Common:4; Rare:139 |