| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103109311-103109564 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106077310-106077706 | Common:2; Rare:118 | ||||
| chr11:107457806-107457934 | Common:1; Rare:39 | ||||
| chr11:108009273-108009349 | Rare:38 | ||||
| chr11:108222603-108223142 | Common:1; Rare:169; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108664828-108665106 | Common:5; Rare:109 | ||||
| chr11:110296577-110296778 | Rare:109; Clinvar:5 | ||||
| chr11:111766345-111766433 | Common:1; Rare:52 | ||||
| chr11:111878886-111878973 | Common:1; Rare:30 | ||||
| chr11:111879152-111879494 | Rare:101 | ||||
| chr11:112074011-112074349 | Common:1; Rare:68 | ||||
| chr11:112086729-112086905 | Rare:71; Clinvar:1 | ||||
| chr11:113314411-113314598 | Rare:66 | ||||
| chr11:113875512-113875815 | Common:4; Rare:115 | ||||
| chr11:114400456-114400753 | Common:2; Rare:118 |