| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127064793-127065013 | Rare:56 | ||||
| chr2:127294094-127294243 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526410-127526607 | Common:2; Rare:72 | ||||
| chr2:127811133-127811258 | Rare:40 | ||||
| chr2:127858102-127858219 | Common:1; Rare:60 | ||||
| chr2:127885896-127885994 | Rare:27 | ||||
| chr2:128091057-128091349 | Common:8; Rare:96 | ||||
| chr2:130181546-130181700 | Common:1; Rare:54 | ||||
| chr2:130182079-130182318 | Common:2; Rare:88 | ||||
| chr2:130342127-130342228 | Rare:39 | ||||
| chr2:130342645-130342930 | Common:5; Rare:89 | ||||
| chr2:131492762-131493092 | Common:8; Rare:99 | ||||
| chr2:134918632-134918886 | Common:1; Rare:114 | ||||
| chr2:135531178-135531526 | Common:1; Rare:72 | ||||
| chr2:135876400-135876633 | Rare:63 |