| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217905415-217905688 | Rare:56 | ||||
| chr2:218217057-218217246 | Common:1; Rare:67 | ||||
| chr2:218270054-218270568 | Common:5; Rare:162; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218287260-218287371 | Rare:20 | ||||
| chr2:218322982-218323296 | Common:6; Rare:103 | ||||
| chr2:218381934-218382308 | Common:1; Rare:70 | ||||
| chr2:218399544-218399665 | Common:1; Rare:48 | ||||
| chr2:218568301-218568592 | Common:2; Rare:77 | ||||
| chr2:218568756-218568955 | Common:1; Rare:60 | ||||
| chr2:218659339-218659363 | Rare:8 | ||||
| chr2:218659474-218659738 | Common:2; Rare:63 | ||||
| chr2:218671973-218672348 | Common:2; Rare:93 | ||||
| chr2:219176842-219177068 | Common:4; Rare:68 | ||||
| chr2:219178142-219178464 | Common:6; Rare:134 | ||||
| chr2:219206678-219206929 | Rare:92 |