| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127885886-127885995 | Rare:29 | ||||
| chr2:128091055-128091360 | Common:8; Rare:99 | ||||
| chr2:130181553-130181749 | Common:2; Rare:87 | ||||
| chr2:130182087-130182336 | Common:2; Rare:96 | ||||
| chr2:130342121-130342281 | Rare:65; Clinvar:1 | ||||
| chr2:130342644-130342924 | Common:5; Rare:85 | ||||
| chr2:131093382-131093559 | Common:1; Rare:83 | ||||
| chr2:131105193-131105356 | Common:1; Rare:70 | ||||
| chr2:131492048-131492219 | Common:3; Rare:50 | ||||
| chr2:131492762-131493097 | Common:8; Rare:101 | ||||
| chr2:134918597-134918862 | Common:1; Rare:105 | ||||
| chr2:135531172-135531508 | Common:1; Rare:70 | ||||
| chr2:136118107-136118328 | Rare:56 | ||||
| chr2:148020681-148021109 | Common:2; Rare:99; Clinvar (benign):2 | ||||
| chr2:148021552-148021658 | Rare:21 |