| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269966-47270242 | Common:2; Rare:93 | ||||
| chr11:47408354-47408655 | Common:1; Rare:94; Clinvar (benign):2 | ||||
| chr11:47426406-47426648 | Rare:60 | ||||
| chr11:47565446-47565752 | Common:4; Rare:67 | ||||
| chr11:47578931-47579085 | Rare:83; Clinvar:2 | ||||
| chr11:47642444-47642668 | Rare:99 | ||||
| chr11:47767067-47767410 | Common:6; Rare:142 | ||||
| chr11:47848298-47848406 | Common:1; Rare:58 | ||||
| chr11:57311431-57311724 | Common:1; Rare:77 | ||||
| chr11:57324877-57325169 | Common:1; Rare:96 | ||||
| chr11:57427049-57427214 | Common:1; Rare:53 | ||||
| chr11:57530675-57531090 | Common:1; Rare:98 | ||||
| chr11:57567589-57567732 | Rare:51 | ||||
| chr11:57657435-57657796 | Common:4; Rare:91 | ||||
| chr11:57712175-57712671 | Common:9; Rare:171 |