| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65575857-65576071 | Common:3; Rare:63 | ||||
| chr11:65614186-65614266 | Rare:21 | ||||
| chr11:65662897-65663012 | Common:1; Rare:30 | ||||
| chr11:65860157-65860765 | Common:3; Rare:197 | ||||
| chr11:65861218-65861314 | Common:2; Rare:28 | ||||
| chr11:65888402-65888640 | Common:1; Rare:87 | ||||
| chr11:65919070-65919294 | Rare:82 | ||||
| chr11:66002097-66002511 | Common:3; Rare:117; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:66289000-66289399 | Common:1; Rare:97 | ||||
| chr11:66335646-66335790 | Common:1; Rare:50 | ||||
| chr11:66336385-66336484 | Rare:26 | ||||
| chr11:66347591-66347816 | Common:3; Rare:56 | ||||
| chr11:66480236-66480447 | Common:1; Rare:56 | ||||
| chr11:66616398-66616666 | Common:1; Rare:78 | ||||
| chr11:66638438-66638718 | Common:2; Rare:117 |