| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197499783-197500725 | Common:2; Rare:331; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515829-197516107 | Common:2; Rare:100 | ||||
| chr2:197705170-197705424 | Common:3; Rare:118; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:199456048-199456180 | Rare:30 | ||||
| chr2:199457501-199457633 | Rare:28 | ||||
| chr2:199911104-199911451 | Rare:122 | ||||
| chr2:200306760-200306907 | Rare:43 | ||||
| chr2:200509866-200510239 | Common:2; Rare:131 | ||||
| chr2:200526010-200526250 | Common:3; Rare:74 | ||||
| chr2:200811408-200811596 | Common:1; Rare:63 | ||||
| chr2:200864214-200864252 | Rare:11 | ||||
| chr2:200864621-200864825 | Rare:80 | ||||
| chr2:200888970-200889510 | Common:3; Rare:168 | ||||
| chr2:200962966-200963311 | Common:1; Rare:51 | ||||
| chr2:200963575-200963893 | Common:1; Rare:83 |