| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65133036-65133250 | Rare:47 | ||||
| chr11:65133347-65133549 | Common:1; Rare:54 | ||||
| chr11:65134392-65134703 | Common:5; Rare:181 | ||||
| chr11:65134772-65134909 | Rare:55 | ||||
| chr11:65134820-65135417 | Common:2; Rare:289 | ||||
| chr11:65170074-65170281 | Common:2; Rare:76 | ||||
| chr11:65181199-65181445 | Common:3; Rare:139 | ||||
| chr11:65181525-65182060 | Common:9; Rare:410 | ||||
| chr11:65182302-65182557 | Common:2; Rare:89 | ||||
| chr11:65183603-65183796 | Common:1; Rare:30 | ||||
| chr11:65188545-65189021 | Common:2; Rare:181; Clinvar (pathogenic):2 | ||||
| chr11:65261668-65262136 | Common:11; Rare:350 | ||||
| chr11:65314614-65314949 | Common:2; Rare:255 | ||||
| chr11:65333608-65333921 | Common:3; Rare:302 | ||||
| chr11:65354330-65354880 | Common:3; Rare:339 |