| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66638393-66638735 | Common:4; Rare:151 | ||||
| chr11:66677748-66678018 | Common:1; Rare:105 | ||||
| chr11:66744650-66744801 | Common:1; Rare:58 | ||||
| chr11:67056784-67056894 | Common:1; Rare:35 | ||||
| chr11:67239721-67240014 | Common:1; Rare:60 | ||||
| chr11:67303347-67303588 | Rare:65 | ||||
| chr11:67317767-67317877 | Rare:19 | ||||
| chr11:67353294-67353376 | Rare:25 | ||||
| chr11:67353473-67353722 | Common:1; Rare:64 | ||||
| chr11:67401730-67402075 | Common:3; Rare:125 | ||||
| chr11:67428307-67428531 | Rare:77 | ||||
| chr11:67443451-67443604 | Common:1; Rare:55 | ||||
| chr11:67469205-67469410 | Common:1; Rare:67 | ||||
| chr11:67482913-67483192 | Rare:62; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508038-67508489 | Common:1; Rare:103 |