| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:20049283-20049339 | Rare:5 | ||||
| chr11:20049342-20049391 | Rare:9 | ||||
| chr11:20049452-20049539 | Rare:8 | ||||
| chr11:33290438-33290549 | Rare:18 | ||||
| chr11:35380703-35380812 | Rare:21 | ||||
| chr11:47160967-47161144 | Rare:49 | ||||
| chr11:47331844-47332260 | Common:1; Rare:129; Clinvar:18; Clinvar (benign):14; Clinvar (pathogenic):10 | ||||
| chr11:47332564-47332833 | Rare:76; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
| chr11:47333270-47333755 | Common:1; Rare:158; Clinvar:21; Clinvar (benign):18; Clinvar (pathogenic):13 | ||||
| chr11:47339649-47340078 | Rare:113; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr11:47341002-47341181 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):3 | ||||
| chr11:47343253-47343749 | Common:7; Rare:137; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
| chr11:47345205-47345448 | Rare:47 | ||||
| chr11:47345839-47346432 | Common:1; Rare:142; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):11 | ||||
| chr11:47346437-47346651 | Common:2; Rare:42; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |