| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130372088-130372281 | Common:2; Rare:52 | ||||
| chr2:130372339-130372766 | Common:3; Rare:119 | ||||
| chr2:131093120-131093247 | Rare:46 | ||||
| chr2:131093501-131093865 | Common:1; Rare:116 | ||||
| chr2:131104913-131105409 | Common:5; Rare:162 | ||||
| chr2:131491579-131491734 | Common:2; Rare:31 | ||||
| chr2:131492091-131492158 | Common:2; Rare:15 | ||||
| chr2:131492620-131493159 | Common:10; Rare:157 | ||||
| chr2:131527751-131528116 | Common:4; Rare:96 | ||||
| chr2:134119783-134120032 | Common:2; Rare:76 | ||||
| chr2:134918154-134918354 | Common:4; Rare:62 | ||||
| chr2:134918653-134918925 | Common:1; Rare:123 | ||||
| chr2:135052073-135052415 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:135052525-135052850 | Common:1; Rare:62 | ||||
| chr2:135530473-135530598 | Rare:24 |