Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124989681-124989966 | Rare:67 | ||||
chr10:131949216-131949486 | Rare:57 | ||||
chr10:131970932-131971087 | Rare:41 | ||||
chr11:318449-318651 | Rare:20 | ||||
chr11:319515-319758 | Common:1; Rare:65 | ||||
chr11:1753512-1753890 | Common:3; Rare:153; Clinvar:11; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
chr11:2653147-2653393 | Common:1; Rare:47 | ||||
chr11:2669572-2669865 | Common:2; Rare:51 | ||||
chr11:10508231-10508265 | Rare:11 | ||||
chr11:12814010-12814290 | Common:1; Rare:63 | ||||
chr11:26995066-26995580 | Rare:103 | ||||
chr11:43471282-43471547 | Rare:57 | ||||
chr11:45903848-45904005 | Rare:26 | ||||
chr11:45904318-45904472 | Rare:37 | ||||
chr11:45904627-45904795 | Rare:51 |