| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201642620-201642740 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr2:201854580-201854794 | Common:2; Rare:46 | ||||
| chr2:202911886-202912283 | Common:2; Rare:108 | ||||
| chr2:203535261-203535504 | Common:2; Rare:100 | ||||
| chr2:206159342-206159925 | Common:4; Rare:157; Clinvar (benign):1 | ||||
| chr2:206765294-206765675 | Common:3; Rare:101; Clinvar:5; Clinvar (benign):6 | ||||
| chr2:207165779-207166094 | Rare:61 | ||||
| chr2:207529747-207530118 | Common:3; Rare:105 | ||||
| chr2:207625216-207625493 | Common:1; Rare:78 | ||||
| chr2:208255024-208255238 | Common:2; Rare:57 | ||||
| chr2:208266064-208266391 | Common:8; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210477535-210477716 | Rare:53 | ||||
| chr2:213151583-213151690 | Rare:33 | ||||
| chr2:213284210-213284481 | Rare:86 | ||||
| chr2:215365356-215365513 | Common:2; Rare:28 |