| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:181457894-181458512 | Common:3; Rare:190 | ||||
| chr2:181656619-181656815 | Common:1; Rare:93; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:181656964-181657005 | Rare:17; Clinvar:3 | ||||
| chr2:181891609-181891859 | Common:4; Rare:114 | ||||
| chr2:181892100-181892215 | Common:1; Rare:34 | ||||
| chr2:181892654-181892812 | Common:1; Rare:51 | ||||
| chr2:182715829-182716416 | Common:3; Rare:183 | ||||
| chr2:183038236-183038360 | Common:1; Rare:37 | ||||
| chr2:183038400-183038648 | Common:4; Rare:79 | ||||
| chr2:183078467-183078880 | Rare:91 | ||||
| chr2:183124069-183124157 | Common:1; Rare:17 | ||||
| chr2:183124233-183124575 | Common:4; Rare:110 | ||||
| chr2:183124776-183124980 | Common:2; Rare:46 | ||||
| chr2:184598339-184598621 | Common:2; Rare:84 | ||||
| chr2:186485698-186486399 | Common:3; Rare:164 |