Variant report

Variant rs565902479
Chromosome Location chr1:47007784-47007785
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:46999600-47035000 Weak transcription Right Atrium heart
2 chr1:47004200-47009200 Weak transcription K562 blood
3 chr1:47006400-47007800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:47006400-47007800 Weak transcription Brain Inferior Temporal Lobe brain
5 chr1:47006600-47007800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr1:47006800-47008400 Enhancers Cortex derived primary cultured neurospheres brain
7 chr1:47007400-47009800 Bivalent Enhancer Fetal Brain Male brain
8 chr1:47007600-47007800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:47007600-47008000 Bivalent Enhancer Liver Liver
10 chr1:47007600-47008000 Bivalent Enhancer Brain Hippocampus Middle brain
11 chr1:47007600-47008000 Enhancers Brain Substantia Nigra brain
12 chr1:47007600-47008200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr1:47007600-47008200 Enhancers Brain Anterior Caudate brain
14 chr1:47007600-47008600 Enhancers Brain Cingulate Gyrus brain
15 chr1:47007600-47008600 Enhancers Brain Dorsolateral Prefrontal Cortex brain

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