| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62612902-62612952 | Rare:14 | ||||
| chr11:62621630-62621757 | Rare:27 | ||||
| chr11:62621798-62622419 | Common:4; Rare:192 | ||||
| chr11:62646175-62646353 | Common:3; Rare:52 | ||||
| chr11:62646357-62646407 | Rare:13 | ||||
| chr11:62646514-62646773 | Common:1; Rare:108; Clinvar (pathogenic):1 | ||||
| chr11:62646808-62646830 | Common:1; Rare:9 | ||||
| chr11:62652988-62653098 | Common:1; Rare:33 | ||||
| chr11:62653215-62653670 | Common:1; Rare:114 | ||||
| chr11:62664484-62664726 | Common:1; Rare:46 | ||||
| chr11:62664728-62664867 | Common:2; Rare:38 | ||||
| chr11:62664899-62665001 | Rare:40 | ||||
| chr11:62665105-62665603 | Common:7; Rare:231 | ||||
| chr11:62665613-62665644 | Common:1; Rare:7 | ||||
| chr11:62671144-62671316 | Common:1; Rare:50 |