| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342647-130342930 | Common:5; Rare:89 | ||||
| chr2:131093374-131093559 | Common:1; Rare:85 | ||||
| chr2:131105253-131105365 | Common:1; Rare:55 | ||||
| chr2:131492276-131492471 | Common:3; Rare:81 | ||||
| chr2:131492754-131493097 | Common:8; Rare:103 | ||||
| chr2:134918576-134918877 | Common:1; Rare:124 | ||||
| chr2:135531219-135531507 | Common:1; Rare:52 | ||||
| chr2:135741640-135741944 | Common:3; Rare:115 | ||||
| chr2:135985404-135985642 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr2:135985653-135985704 | Rare:15 | ||||
| chr2:138501679-138502005 | Common:2; Rare:109 | ||||
| chr2:144430757-144430833 | Rare:12 | ||||
| chr2:144518134-144518199 | Common:1; Rare:12 | ||||
| chr2:148020673-148021109 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr2:148021579-148021624 | Rare:11 |