| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:128091038-128091338 | Common:8; Rare:101 | ||||
| chr2:130181546-130181797 | Common:3; Rare:111 | ||||
| chr2:130182101-130182347 | Common:2; Rare:97 | ||||
| chr2:130342123-130342244 | Rare:51; Clinvar:1 | ||||
| chr2:130342352-130342410 | Rare:17 | ||||
| chr2:130342686-130342935 | Common:3; Rare:81 | ||||
| chr2:130756119-130756344 | Common:2; Rare:78 | ||||
| chr2:131105193-131105385 | Common:2; Rare:88 | ||||
| chr2:131492734-131493097 | Common:8; Rare:108 | ||||
| chr2:132257951-132257992 | Common:1; Rare:6 | ||||
| chr2:134918225-134918297 | Common:1; Rare:18 | ||||
| chr2:134918585-134918886 | Common:1; Rare:127 | ||||
| chr2:135052168-135052314 | Common:1; Rare:53; Clinvar (benign):1 | ||||
| chr2:135531178-135531526 | Common:1; Rare:72 | ||||
| chr2:135741716-135741937 | Common:1; Rare:87 |