| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65961684-65961758 | Rare:28 | ||||
| chr11:66002079-66002847 | Common:4; Rare:217; Clinvar:8; Clinvar (benign):3 | ||||
| chr11:66021107-66021274 | Rare:46; Clinvar:1 | ||||
| chr11:66257613-66257773 | Rare:37 | ||||
| chr11:66258388-66258447 | Rare:13 | ||||
| chr11:66268404-66268674 | Common:3; Rare:78 | ||||
| chr11:66289072-66289398 | Common:1; Rare:77 | ||||
| chr11:66336669-66336984 | Rare:55 | ||||
| chr11:66345036-66345203 | Common:1; Rare:49 | ||||
| chr11:66480212-66480462 | Common:3; Rare:67 | ||||
| chr11:66593053-66593209 | Common:1; Rare:54 | ||||
| chr11:66616396-66616646 | Common:1; Rare:68 | ||||
| chr11:66638369-66638747 | Common:4; Rare:169 | ||||
| chr11:66677791-66678125 | Common:1; Rare:117 | ||||
| chr11:66744652-66744879 | Common:3; Rare:94 |