| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102317104-102317521 | Common:1; Rare:69 | ||||
| chr11:102347111-102347336 | Common:2; Rare:76 | ||||
| chr11:102452523-102452943 | Common:2; Rare:139 | ||||
| chr11:105045314-105045404 | Rare:26 | ||||
| chr11:106022178-106022532 | Common:3; Rare:107 | ||||
| chr11:106077326-106077706 | Common:2; Rare:113 | ||||
| chr11:108009302-108009356 | Rare:26 | ||||
| chr11:108121390-108121621 | Common:5; Rare:79; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:108222573-108223128 | Common:1; Rare:179; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108467494-108467620 | Common:3; Rare:46 | ||||
| chr11:110296498-110296779 | Common:1; Rare:133; Clinvar:8 | ||||
| chr11:111299674-111299769 | Common:2; Rare:24 | ||||
| chr11:111541460-111541555 | Common:1; Rare:20 | ||||
| chr11:111602185-111602572 | Common:1; Rare:124 | ||||
| chr11:111766345-111766439 | Common:1; Rare:57 |