| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108009312-108009349 | Rare:21 | ||||
| chr11:108121419-108121601 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108222609-108223128 | Common:1; Rare:161; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108664831-108665120 | Common:5; Rare:114 | ||||
| chr11:110296507-110296802 | Common:1; Rare:137; Clinvar:7 | ||||
| chr11:111766363-111766433 | Common:1; Rare:39 | ||||
| chr11:111871544-111871625 | Rare:27 | ||||
| chr11:111878815-111878950 | Common:2; Rare:32 | ||||
| chr11:111879456-111879562 | Common:1; Rare:39 | ||||
| chr11:111912531-111912796 | Common:1; Rare:55 | ||||
| chr11:112074018-112074377 | Common:1; Rare:77 | ||||
| chr11:112086726-112086907 | Rare:75; Clinvar:1 | ||||
| chr11:112226287-112226450 | Rare:70 | ||||
| chr11:112961143-112961545 | Common:2; Rare:156 | ||||
| chr11:113875491-113875799 | Common:4; Rare:117 |