| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66002093-66002420 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:66002458-66002818 | Common:1; Rare:100; Clinvar:1 | ||||
| chr11:66060561-66060597 | Rare:10 | ||||
| chr11:66257893-66258166 | Common:2; Rare:68 | ||||
| chr11:66260450-66260548 | Rare:15 | ||||
| chr11:66268335-66268679 | Common:3; Rare:99 | ||||
| chr11:66268823-66268909 | Rare:24 | ||||
| chr11:66288987-66289237 | Common:1; Rare:66 | ||||
| chr11:66344978-66345386 | Common:1; Rare:107 | ||||
| chr11:66347421-66347933 | Common:7; Rare:124; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:66372083-66372258 | Common:2; Rare:38 | ||||
| chr11:66438689-66439199 | Common:4; Rare:131 | ||||
| chr11:66466525-66466942 | Common:2; Rare:118 | ||||
| chr11:66480227-66480478 | Common:1; Rare:68 | ||||
| chr11:66545966-66546301 | Common:5; Rare:86 |