Variant report

Variant rs4656668
Chromosome Location chr1:169210739-169210740
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169172600-169227000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:169187800-169211800 Weak transcription Primary hematopoietic stem cells blood
3 chr1:169194800-169214000 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr1:169199200-169211600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr1:169201000-169212800 Weak transcription Psoas Muscle Psoas
6 chr1:169208000-169214400 Weak transcription Ovary ovary
7 chr1:169209600-169210800 Enhancers NHEK skin
8 chr1:169209800-169210800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr1:169209800-169210800 Enhancers Liver Liver
10 chr1:169210200-169210800 Enhancers Rectal Smooth Muscle rectum
11 chr1:169210400-169210800 Enhancers NHDF-Ad bronchial
12 chr1:169210400-169214400 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr1:169210600-169211800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr1:169210600-169211800 Weak transcription A549 lung
15 chr1:169210600-169215400 Weak transcription Stomach Mucosa stomach

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