| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66345003-66345203 | Common:1; Rare:54 | ||||
| chr11:66347611-66347834 | Common:5; Rare:55 | ||||
| chr11:66371731-66372028 | Common:1; Rare:77 | ||||
| chr11:66480212-66480455 | Common:3; Rare:65 | ||||
| chr11:66510549-66510687 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66593081-66593223 | Common:1; Rare:53 | ||||
| chr11:66616385-66616657 | Common:1; Rare:81 | ||||
| chr11:66638393-66638752 | Common:4; Rare:157 | ||||
| chr11:66677769-66677981 | Common:1; Rare:81 | ||||
| chr11:66744623-66744859 | Common:3; Rare:100 | ||||
| chr11:66843320-66843506 | Common:5; Rare:94 | ||||
| chr11:67056784-67056893 | Common:1; Rare:34 | ||||
| chr11:67239812-67240134 | Rare:65 | ||||
| chr11:67303343-67303582 | Rare:61 | ||||
| chr11:67317676-67317943 | Rare:66 |