| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:44095586-44095753 | Common:1; Rare:50; Clinvar (benign):2 | ||||
| chr11:45286074-45286437 | Rare:106 | ||||
| chr11:45885557-45885860 | Common:3; Rare:95 | ||||
| chr11:45917824-45918190 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46593997-46594133 | Common:2; Rare:28 | ||||
| chr11:46617165-46617585 | Common:5; Rare:118 | ||||
| chr11:46700553-46700839 | Common:1; Rare:74 | ||||
| chr11:46700925-46701077 | Common:2; Rare:42 | ||||
| chr11:46846138-46846421 | Common:1; Rare:91 | ||||
| chr11:47176837-47177138 | Common:1; Rare:126 | ||||
| chr11:47214843-47215003 | Common:1; Rare:42 | ||||
| chr11:47248785-47248959 | Rare:72 | ||||
| chr11:47269083-47269390 | Common:1; Rare:63 | ||||
| chr11:47269556-47269864 | Common:1; Rare:107 | ||||
| chr11:47269966-47270223 | Common:1; Rare:89 |