| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:128091055-128091335 | Common:8; Rare:95 | ||||
| chr2:130181553-130181795 | Common:3; Rare:106 | ||||
| chr2:130182031-130182381 | Common:2; Rare:129 | ||||
| chr2:130342104-130342244 | Rare:63; Clinvar:1 | ||||
| chr2:130342642-130342930 | Common:5; Rare:90 | ||||
| chr2:131105045-131105367 | Common:2; Rare:105 | ||||
| chr2:131492066-131492425 | Common:7; Rare:134 | ||||
| chr2:131492749-131492967 | Common:4; Rare:71 | ||||
| chr2:131493019-131493097 | Common:1; Rare:22 | ||||
| chr2:134918588-134918863 | Common:1; Rare:110 | ||||
| chr2:135052192-135052317 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr2:135531172-135531508 | Common:1; Rare:70 | ||||
| chr2:135741586-135741945 | Common:5; Rare:125 | ||||
| chr2:135985407-135985708 | Common:4; Rare:129; Clinvar (benign):1 | ||||
| chr2:135985870-135985977 | Common:1; Rare:26 |