| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:107457753-107457932 | Common:2; Rare:60 | ||||
| chr11:107591063-107591376 | Common:2; Rare:101 | ||||
| chr11:108009304-108009357 | Rare:25 | ||||
| chr11:108121404-108121614 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108222577-108223128 | Common:1; Rare:176; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223405-108223434 | Rare:8 | ||||
| chr11:110296641-110296788 | Rare:78; Clinvar:3 | ||||
| chr11:110712297-110712571 | Common:2; Rare:106 | ||||
| chr11:111299673-111299769 | Common:2; Rare:24 | ||||
| chr11:111602226-111602562 | Common:1; Rare:113 | ||||
| chr11:111766338-111766415 | Rare:46 | ||||
| chr11:111871302-111871376 | Rare:31; Clinvar:1 | ||||
| chr11:111878697-111878973 | Common:2; Rare:76 | ||||
| chr11:111879152-111879541 | Rare:117 | ||||
| chr11:111913128-111913260 | Rare:40 |