| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190880588-190880859 | Common:4; Rare:95 | ||||
| chr2:191014134-191014353 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245243-191245541 | Common:2; Rare:95 | ||||
| chr2:191246159-191246248 | Rare:32 | ||||
| chr2:191677856-191678147 | Common:4; Rare:82 | ||||
| chr2:191847198-191847476 | Rare:42 | ||||
| chr2:197434973-197435192 | Rare:75 | ||||
| chr2:197453244-197453563 | Rare:110 | ||||
| chr2:197499813-197500191 | Rare:134; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500194-197500420 | Common:1; Rare:95 | ||||
| chr2:200306432-200306562 | Common:2; Rare:27 | ||||
| chr2:200509907-200510218 | Common:1; Rare:108 | ||||
| chr2:200811431-200811572 | Common:1; Rare:50 | ||||
| chr2:200864229-200864252 | Rare:6 | ||||
| chr2:200864569-200864811 | Common:1; Rare:88 |