| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:95402474-95402874 | Rare:491 | ||||
| chr2:95402951-95403351 | Rare:75 | ||||
| chr2:95403288-95403535 | Rare:47 | ||||
| chr2:95991342-95992214 | Common:4; Rare:449 | ||||
| chr2:95992120-95992610 | Common:4; Rare:163 | ||||
| chr2:96116420-96116700 | Common:1; Rare:80 | ||||
| chr2:96208162-96208562 | Rare:781 | ||||
| chr2:96208697-96209244 | Common:30; Rare:730 | ||||
| chr2:96260456-96260856 | Rare:141 | ||||
| chr2:96265850-96266395 | Common:14; Rare:841; Clinvar:15; Clinvar (benign):1 | ||||
| chr2:96304748-96305360 | Rare:165; Clinvar:2 | ||||
| chr2:96305406-96306020 | Common:25; Rare:872; Clinvar:25; Clinvar (benign):16 | ||||
| chr2:96324883-96324984 | Rare:13 | ||||
| chr2:96325070-96325724 | Common:3; Rare:427 | ||||
| chr2:96335586-96335864 | Common:9; Rare:440 |