| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127885822-127886005 | Rare:50 | ||||
| chr2:127886156-127886353 | Common:1; Rare:48 | ||||
| chr2:128091044-128091355 | Common:8; Rare:101 | ||||
| chr2:130181553-130181796 | Common:3; Rare:106 | ||||
| chr2:130182168-130182381 | Common:2; Rare:85 | ||||
| chr2:130342104-130342306 | Rare:86; Clinvar:1 | ||||
| chr2:130342686-130342939 | Common:3; Rare:84 | ||||
| chr2:130355939-130356128 | Common:3; Rare:54 | ||||
| chr2:131093382-131093559 | Common:1; Rare:83 | ||||
| chr2:131105192-131105378 | Common:1; Rare:85 | ||||
| chr2:131492075-131492185 | Common:3; Rare:31 | ||||
| chr2:131492754-131492945 | Common:4; Rare:62 | ||||
| chr2:131493038-131493100 | Common:1; Rare:17 | ||||
| chr2:134918589-134918908 | Common:1; Rare:134 | ||||
| chr2:135052167-135052314 | Common:1; Rare:53; Clinvar (benign):1 |