| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:105035121-105035193 | Rare:23 | ||||
| chr11:106022162-106022564 | Common:3; Rare:116 | ||||
| chr11:106077289-106077711 | Common:2; Rare:128 | ||||
| chr11:107457716-107457949 | Common:3; Rare:78 | ||||
| chr11:107565504-107565787 | Rare:77 | ||||
| chr11:107591055-107591369 | Common:1; Rare:101 | ||||
| chr11:107858551-107858596 | Rare:11 | ||||
| chr11:107928162-107928460 | Common:2; Rare:70 | ||||
| chr11:108008838-108009187 | Common:1; Rare:88 | ||||
| chr11:108009273-108009357 | Rare:40 | ||||
| chr11:108121404-108121621 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:108121725-108121874 | Common:1; Rare:28 | ||||
| chr11:108222589-108223158 | Common:1; Rare:179; Clinvar:9; Clinvar (benign):1 | ||||
| chr11:108223351-108223435 | Rare:24 | ||||
| chr11:108353565-108353848 | Common:1; Rare:51; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 |