Variant report

Variant rs1911074
Chromosome Location chr4:97275585-97275586
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:97274000-97284600 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr4:97275000-97275600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
3 chr4:97275000-97275600 Active TSS Brain Cingulate Gyrus brain
4 chr4:97275000-97275600 Enhancers Brain Hippocampus Middle brain
5 chr4:97275000-97275600 Active TSS Brain Dorsolateral Prefrontal Cortex brain
6 chr4:97275000-97275600 Enhancers Rectal Smooth Muscle rectum
7 chr4:97275000-97275800 Enhancers Brain Substantia Nigra brain
8 chr4:97275000-97275800 Flanking Active TSS Dnd41 blood
9 chr4:97275200-97275600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr4:97275200-97275600 Enhancers Fetal Intestine Large intestine
11 chr4:97275200-97275600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
12 chr4:97275200-97275600 Active TSS Right Atrium heart
13 chr4:97275200-97275600 Enhancers Small Intestine intestine
14 chr4:97275200-97275600 Enhancers Stomach Mucosa stomach
15 chr4:97275200-97275600 Enhancers HUVEC blood vessel
16 chr4:97275400-97275600 Enhancers Brain Anterior Caudate brain
17 chr4:97275400-97275600 Flanking Active TSS Brain Inferior Temporal Lobe brain
18 chr4:97275400-97275600 Enhancers Fetal Kidney kidney

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