| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218381910-218382348 | Common:2; Rare:85 | ||||
| chr2:218399502-218399773 | Common:1; Rare:121 | ||||
| chr2:218568283-218568966 | Common:5; Rare:179 | ||||
| chr2:218659334-218659743 | Common:4; Rare:96 | ||||
| chr2:218667949-218668108 | Rare:39 | ||||
| chr2:218671973-218672348 | Common:2; Rare:93 | ||||
| chr2:218782029-218782334 | Rare:96; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:218984562-218984586 | Rare:8 | ||||
| chr2:218993414-218993641 | Rare:57 | ||||
| chr2:219160545-219160580 | Rare:5 | ||||
| chr2:219176897-219177109 | Common:4; Rare:64 | ||||
| chr2:219177123-219177174 | Rare:7 | ||||
| chr2:219177188-219177202 | Rare:3 | ||||
| chr2:219177813-219177933 | Common:4; Rare:25 | ||||
| chr2:219178136-219178338 | Common:6; Rare:109 |