| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342111-130342270 | Rare:69; Clinvar:1 | ||||
| chr2:130342679-130342929 | Common:3; Rare:82 | ||||
| chr2:131093382-131093511 | Common:1; Rare:64 | ||||
| chr2:131105192-131105362 | Common:1; Rare:75 | ||||
| chr2:131492754-131493107 | Common:8; Rare:108 | ||||
| chr2:134918589-134918857 | Common:1; Rare:105 | ||||
| chr2:135531178-135531514 | Common:1; Rare:70 | ||||
| chr2:135985404-135985642 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr2:138501679-138502002 | Common:2; Rare:108 | ||||
| chr2:144517324-144517709 | Common:5; Rare:115; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144518134-144518197 | Common:1; Rare:9 | ||||
| chr2:144518386-144518506 | Rare:27 | ||||
| chr2:144520047-144520528 | Common:4; Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020692-148021106 | Common:2; Rare:95; Clinvar (benign):2 | ||||
| chr2:149587299-149587347 | Rare:14 |