| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342123-130342281 | Rare:64; Clinvar:1 | ||||
| chr2:130342672-130342930 | Common:4; Rare:82 | ||||
| chr2:131093382-131093569 | Common:1; Rare:87 | ||||
| chr2:131105214-131105356 | Common:1; Rare:60 | ||||
| chr2:131492754-131492959 | Common:4; Rare:66 | ||||
| chr2:131493034-131493097 | Common:1; Rare:16 | ||||
| chr2:134918585-134918870 | Common:1; Rare:115 | ||||
| chr2:135052208-135052325 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135741716-135741956 | Common:1; Rare:92 | ||||
| chr2:135985404-135985670 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr2:135985870-135986084 | Common:1; Rare:45 | ||||
| chr2:137964120-137964515 | Common:2; Rare:65 | ||||
| chr2:138501649-138502026 | Common:4; Rare:137 | ||||
| chr2:144332446-144332633 | Rare:71 |