| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66370742-66370972 | Common:2; Rare:30 | ||||
| chr11:66408400-66408715 | Common:5; Rare:60 | ||||
| chr11:66408970-66409199 | Rare:49 | ||||
| chr11:66437934-66437955 | |||||
| chr11:66438238-66438317 | Rare:20 | ||||
| chr11:66615887-66616007 | Rare:15 | ||||
| chr11:66678542-66678770 | Rare:55 | ||||
| chr11:66851712-66851998 | Rare:102; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:66883295-66883385 | Common:2; Rare:22 | ||||
| chr11:66968209-66968283 | Rare:10 | ||||
| chr11:66970864-66971031 | Common:2; Rare:27 | ||||
| chr11:66982112-66982304 | Rare:39 | ||||
| chr11:66989580-66989744 | Rare:35 | ||||
| chr11:67118235-67118474 | Rare:56 | ||||
| chr11:67180296-67180446 | Rare:33 |