| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68036301-68036518 | Rare:87; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr11:68271930-68272102 | Common:2; Rare:78 | ||||
| chr11:68903791-68903915 | Common:3; Rare:55; Clinvar (benign):2 | ||||
| chr11:69640984-69641225 | Rare:51 | ||||
| chr11:70398281-70398627 | Common:4; Rare:124 | ||||
| chr11:71448295-71448690 | Common:4; Rare:108; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:73876804-73877036 | Common:4; Rare:62 | ||||
| chr11:74171020-74171298 | Common:2; Rare:98 | ||||
| chr11:74949061-74949358 | Common:6; Rare:88 | ||||
| chr11:75562703-75562865 | Common:1; Rare:36 | ||||
| chr11:76783076-76783351 | Common:8; Rare:90 | ||||
| chr11:77820993-77821210 | Common:1; Rare:68 | ||||
| chr11:78079581-78079651 | Common:2; Rare:19 | ||||
| chr11:78139578-78139789 | Common:3; Rare:84; Clinvar:2 | ||||
| chr11:78188614-78188919 | Common:2; Rare:96 |