| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45917787-45917936 | Rare:42; Clinvar:1 | ||||
| chr11:46119770-46120027 | Common:2; Rare:66 | ||||
| chr11:46120936-46121278 | Common:2; Rare:51 | ||||
| chr11:46377895-46377925 | Rare:5 | ||||
| chr11:46382065-46382318 | Common:1; Rare:95 | ||||
| chr11:46617165-46617585 | Common:5; Rare:118 | ||||
| chr11:46617842-46617901 | Rare:12 | ||||
| chr11:46700553-46700862 | Common:1; Rare:83 | ||||
| chr11:46700928-46701083 | Common:2; Rare:46 | ||||
| chr11:46846215-46846421 | Common:1; Rare:59 | ||||
| chr11:46936672-46936808 | Common:2; Rare:46 | ||||
| chr11:47214918-47215210 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248755-47248975 | Common:1; Rare:87 | ||||
| chr11:47268002-47268102 | Rare:30 | ||||
| chr11:47408403-47408628 | Rare:70 |