| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130129373-130129690 | Common:4; Rare:89 | ||||
| chr2:130181546-130181721 | Common:2; Rare:71 | ||||
| chr2:130342123-130342242 | Rare:49; Clinvar:1 | ||||
| chr2:130342681-130342930 | Common:3; Rare:82 | ||||
| chr2:131093382-131093544 | Common:1; Rare:77 | ||||
| chr2:131105233-131105370 | Common:1; Rare:66 | ||||
| chr2:131492748-131493097 | Common:8; Rare:105 | ||||
| chr2:134918585-134918857 | Common:1; Rare:106 | ||||
| chr2:135052214-135052325 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr2:135531178-135531509 | Common:1; Rare:69 | ||||
| chr2:135876371-135876650 | Common:1; Rare:76 | ||||
| chr2:135985404-135985704 | Common:4; Rare:129; Clinvar (benign):1 | ||||
| chr2:136118133-136118328 | Rare:49 | ||||
| chr2:138501664-138502037 | Common:2; Rare:131 | ||||
| chr2:142130842-142130992 | Rare:39 |