| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72793655-72793767 | Rare:30 | ||||
| chr11:72814054-72814458 | Common:4; Rare:121 | ||||
| chr11:73308755-73308924 | Rare:54 | ||||
| chr11:73597986-73598283 | Common:3; Rare:75 | ||||
| chr11:73760577-73760887 | Common:2; Rare:73 | ||||
| chr11:73787760-73787942 | Common:1; Rare:40 | ||||
| chr11:73876804-73877033 | Common:4; Rare:60 | ||||
| chr11:73982814-73982962 | Common:6; Rare:48 | ||||
| chr11:74170845-74171445 | Common:3; Rare:189 | ||||
| chr11:74398373-74398551 | Common:3; Rare:39 | ||||
| chr11:74949055-74949294 | Common:6; Rare:64 | ||||
| chr11:75151227-75151358 | Common:2; Rare:23 | ||||
| chr11:75351593-75351878 | Common:3; Rare:84 | ||||
| chr11:75525907-75526023 | Common:2; Rare:33 | ||||
| chr11:75562053-75562307 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):2 |