Variant report

Variant rs11673114
Chromosome Location chr19:41465979-41465980
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41464800-41466400 Weak transcription Fetal Intestine Small intestine
2 chr19:41465200-41466600 Enhancers Esophagus oesophagus
3 chr19:41465400-41466000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr19:41465800-41466000 Bivalent Enhancer hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr19:41465800-41466000 Flanking Bivalent TSS/Enh Brain Dorsolateral Prefrontal Cortex brain
6 chr19:41465800-41466200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr19:41465800-41466200 Flanking Bivalent TSS/Enh ES-UCSF4 Cell Line embryonic stem cell
8 chr19:41465800-41466200 Flanking Bivalent TSS/Enh Breast Myoepithelial Primary Cells Breast

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