| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191014140-191014353 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677858-191678173 | Common:4; Rare:90 | ||||
| chr2:197434999-197435235 | Rare:75 | ||||
| chr2:197499791-197500430 | Common:2; Rare:242; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515780-197516089 | Common:2; Rare:109 | ||||
| chr2:199911140-199911357 | Rare:64 | ||||
| chr2:200811328-200811572 | Common:1; Rare:75 | ||||
| chr2:200888989-200889451 | Common:3; Rare:144 | ||||
| chr2:201071626-201072043 | Rare:86 | ||||
| chr2:201115944-201116183 | Common:2; Rare:42 | ||||
| chr2:201642627-201642775 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chr2:202238478-202238675 | Rare:69; Clinvar:1 | ||||
| chr2:202265635-202265812 | Rare:69 | ||||
| chr2:202912127-202912281 | Common:2; Rare:53 | ||||
| chr2:203238681-203239026 | Common:1; Rare:100 |