| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181546-130181775 | Common:2; Rare:104 | ||||
| chr2:130182079-130182381 | Common:2; Rare:115 | ||||
| chr2:130342085-130342322 | Rare:97; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:130342699-130342930 | Common:3; Rare:77 | ||||
| chr2:130369693-130369823 | Common:1; Rare:30 | ||||
| chr2:130372551-130372790 | Common:1; Rare:66 | ||||
| chr2:131093382-131093549 | Common:1; Rare:80 | ||||
| chr2:131105233-131105375 | Common:1; Rare:69 | ||||
| chr2:131492754-131492945 | Common:4; Rare:62 | ||||
| chr2:131493034-131493113 | Common:1; Rare:23 | ||||
| chr2:134918185-134918235 | Common:1; Rare:13 | ||||
| chr2:134918585-134918863 | Common:1; Rare:110 | ||||
| chr2:135531172-135531508 | Common:1; Rare:70 | ||||
| chr2:135741602-135741963 | Common:4; Rare:129 | ||||
| chr2:135876352-135876650 | Common:1; Rare:84 |