| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108222068-108222135 | Rare:11 | ||||
| chr11:108222552-108222941 | Rare:133; Clinvar:2 | ||||
| chr11:108222997-108223142 | Common:1; Rare:42; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:108223144-108223204 | Rare:13; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:108223205-108223340 | Rare:35 | ||||
| chr11:108223969-108224107 | Rare:29 | ||||
| chr11:108467372-108467698 | Common:4; Rare:114 | ||||
| chr11:108498172-108498578 | Common:5; Rare:121 | ||||
| chr11:108664788-108665156 | Common:6; Rare:146 | ||||
| chr11:110093036-110093181 | Common:1; Rare:40 | ||||
| chr11:110093702-110093853 | Common:5; Rare:54 | ||||
| chr11:110296492-110296871 | Common:3; Rare:161; Clinvar:8 | ||||
| chr11:110429813-110429896 | Common:2; Rare:25 | ||||
| chr11:110429902-110430197 | Common:4; Rare:82 | ||||
| chr11:110712389-110712563 | Common:1; Rare:62 |