| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67465277-67465307 | Rare:6 | ||||
| chr11:67468183-67468233 | Common:1; Rare:9 | ||||
| chr11:67469115-67469340 | Common:2; Rare:86 | ||||
| chr11:67482954-67483192 | Rare:54; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:67507794-67507877 | Rare:19 | ||||
| chr11:67508014-67508295 | Common:1; Rare:76 | ||||
| chr11:67583433-67583895 | Common:8; Rare:124 | ||||
| chr11:67607578-67607743 | Common:3; Rare:32 | ||||
| chr11:67612115-67612507 | Common:2; Rare:147; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68030597-68030966 | Common:7; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68213265-68213719 | Common:1; Rare:238 | ||||
| chr11:68271891-68272171 | Common:2; Rare:121 | ||||
| chr11:68460560-68460830 | Common:3; Rare:91 | ||||
| chr11:68841799-68841844 | Common:1; Rare:20; Clinvar (benign):2 | ||||
| chr11:68903725-68903961 | Common:5; Rare:105; Clinvar:3; Clinvar (benign):7 |