| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65961490-65961818 | Common:1; Rare:108 | ||||
| chr11:65962011-65962181 | Common:3; Rare:69 | ||||
| chr11:66002067-66002826 | Common:4; Rare:209; Clinvar:8; Clinvar (benign):3 | ||||
| chr11:66002896-66003188 | Common:4; Rare:73 | ||||
| chr11:66021142-66021249 | Rare:31 | ||||
| chr11:66051805-66052178 | Common:5; Rare:94 | ||||
| chr11:66052180-66052590 | Common:5; Rare:136 | ||||
| chr11:66052744-66052813 | Rare:19 | ||||
| chr11:66070030-66070162 | Common:1; Rare:34 | ||||
| chr11:66070175-66070442 | Common:1; Rare:84 | ||||
| chr11:66070687-66070800 | Rare:29; Clinvar (benign):1 | ||||
| chr11:66257523-66257728 | Rare:54 | ||||
| chr11:66257734-66258040 | Common:1; Rare:86 | ||||
| chr11:66258330-66258528 | Rare:43 | ||||
| chr11:66267537-66268060 | Common:7; Rare:142 |