| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3558211-3558695 | Common:6; Rare:182 | ||||
| chr2:3575098-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:6866551-6866675 | Rare:19 | ||||
| chr2:9003957-9004090 | Rare:56 | ||||
| chr2:9422796-9422838 | Rare:5 | ||||
| chr2:9423108-9423697 | Common:2; Rare:156 | ||||
| chr2:9473486-9473776 | Common:1; Rare:64 | ||||
| chr2:9474493-9474642 | Common:6; Rare:71 | ||||
| chr2:9555621-9555966 | Common:2; Rare:115 | ||||
| chr2:9630944-9631316 | Common:3; Rare:119 | ||||
| chr2:9843254-9843553 | Common:6; Rare:89 | ||||
| chr2:10302746-10302918 | Common:2; Rare:60 | ||||
| chr2:10368588-10368702 | Common:1; Rare:16 | ||||
| chr2:10419647-10419799 | Rare:42 | ||||
| chr2:10689892-10690018 | Common:2; Rare:48 |