| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342022-130342279 | Rare:103; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr2:130342686-130342933 | Common:3; Rare:80 | ||||
| chr2:130836766-130836972 | Common:2; Rare:84 | ||||
| chr2:131093358-131093559 | Common:1; Rare:93 | ||||
| chr2:131105274-131105375 | Common:1; Rare:52 | ||||
| chr2:131492048-131492219 | Common:3; Rare:50 | ||||
| chr2:131492762-131493118 | Common:8; Rare:109 | ||||
| chr2:134918588-134918863 | Common:1; Rare:110 | ||||
| chr2:135052159-135052316 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr2:135531172-135531521 | Common:1; Rare:74 | ||||
| chr2:135741605-135741950 | Common:4; Rare:123 | ||||
| chr2:135985092-135985219 | Rare:35 | ||||
| chr2:135985403-135985689 | Common:4; Rare:126; Clinvar (benign):1 | ||||
| chr2:135985692-135985792 | Common:1; Rare:34 | ||||
| chr2:136118147-136118329 | Rare:49 |