Variant report

Variant rs4097641
Chromosome Location chr9:104250455-104250456
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:104249800-104250800 Enhancers Fetal Heart heart
2 chr9:104250000-104250600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr9:104250000-104250600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr9:104250000-104250600 Enhancers Brain Inferior Temporal Lobe brain
5 chr9:104250000-104250600 Enhancers Fetal Intestine Small intestine
6 chr9:104250000-104250600 Enhancers Stomach Mucosa stomach
7 chr9:104250000-104250800 Enhancers Fetal Intestine Large intestine
8 chr9:104250000-104250800 Enhancers NHEK skin
9 chr9:104250000-104253600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr9:104250200-104250600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr9:104250200-104250800 Enhancers Pancreatic Islets Pancreatic Islet
12 chr9:104250400-104250600 Enhancers Brain Angular Gyrus brain

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