| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95923824-95924157 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389862-96390043 | Common:1; Rare:72 | ||||
| chr11:101914869-101915025 | Common:1; Rare:40 | ||||
| chr11:102347105-102347279 | Common:2; Rare:50 | ||||
| chr11:102452659-102452944 | Common:1; Rare:90 | ||||
| chr11:103092083-103092262 | Common:1; Rare:63 | ||||
| chr11:106077335-106077704 | Common:2; Rare:110 | ||||
| chr11:107457753-107457940 | Common:2; Rare:64 | ||||
| chr11:108009260-108009350 | Rare:45 | ||||
| chr11:108222568-108222956 | Rare:133; Clinvar:3 | ||||
| chr11:108223004-108223128 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:108467506-108467595 | Rare:27 | ||||
| chr11:108664880-108665116 | Common:5; Rare:90 | ||||
| chr11:110130733-110131004 | Rare:59 | ||||
| chr11:111766345-111766426 | Rare:42 |