| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:849160-850137 | Common:15; Rare:490 | ||||
| chr11:910125-910700 | Common:1; Rare:171 | ||||
| chr11:910740-911115 | Common:11; Rare:336 | ||||
| chr11:925685-925971 | Common:7; Rare:326 | ||||
| chr11:1036630-1036901 | Rare:79 | ||||
| chr11:1222760-1223194 | Common:10; Rare:159 | ||||
| chr11:1309535-1309867 | Common:8; Rare:385 | ||||
| chr11:1389511-1390070 | Common:7; Rare:271 | ||||
| chr11:1559420-1559810 | Common:4; Rare:76 | ||||
| chr11:1572045-1572820 | Common:11; Rare:452 | ||||
| chr11:1749010-1749276 | Common:6; Rare:166 | ||||
| chr11:1749963-1750279 | Common:5; Rare:105 | ||||
| chr11:1750545-1750722 | Common:6; Rare:56 | ||||
| chr11:1761290-1761801 | Common:7; Rare:254; Clinvar:18; Clinvar (benign):23 | ||||
| chr11:1762338-1762699 | Common:9; Rare:214 |