| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95923761-95923876 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:95923939-95924149 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:96389602-96389787 | Common:2; Rare:54 | ||||
| chr11:96389842-96390052 | Common:1; Rare:87 | ||||
| chr11:99020623-99021075 | Rare:128 | ||||
| chr11:100687694-100687769 | Rare:9 | ||||
| chr11:101127523-101127725 | Rare:89 | ||||
| chr11:101583435-101583609 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:101583906-101584087 | Rare:46; Clinvar:1 | ||||
| chr11:101914752-101915093 | Common:4; Rare:81 | ||||
| chr11:101915106-101915357 | Common:3; Rare:72 | ||||
| chr11:102110218-102110471 | Common:1; Rare:99 | ||||
| chr11:102110634-102111162 | Common:5; Rare:173; Clinvar:1 | ||||
| chr11:102317254-102317563 | Rare:65 | ||||
| chr11:102347011-102347463 | Common:10; Rare:125 |