| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65524793-65525144 | Rare:66 | ||||
| chr11:65570413-65570494 | Rare:36 | ||||
| chr11:65662884-65663006 | Common:1; Rare:35 | ||||
| chr11:65860430-65860742 | Common:2; Rare:97 | ||||
| chr11:65872735-65872961 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:65888109-65888532 | Common:1; Rare:138; Clinvar:1 | ||||
| chr11:65890454-65890690 | Common:4; Rare:76 | ||||
| chr11:66002120-66002818 | Common:4; Rare:198; Clinvar:4; Clinvar (benign):3 | ||||
| chr11:66289041-66289393 | Common:1; Rare:83 | ||||
| chr11:66345049-66345216 | Common:1; Rare:46 | ||||
| chr11:66347626-66347869 | Common:5; Rare:56 | ||||
| chr11:66480239-66480448 | Common:1; Rare:55 | ||||
| chr11:66616403-66616646 | Common:1; Rare:64 | ||||
| chr11:66677796-66677981 | Common:1; Rare:70 | ||||
| chr11:67353518-67353890 | Common:2; Rare:92 |