Variant report

Variant	rs16962293
Chromosome Location	chr17:63397637-63397638
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:63390200-63398600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:63396800-63397800	Enhancers	Brain Germinal Matrix	brain
3	chr17:63396800-63400800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr17:63397000-63398000	Enhancers	Duodenum Mucosa	Duodenum
5	chr17:63397000-63399200	Enhancers	Fetal Lung	lung
6	chr17:63397400-63399600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr17:63397600-63398000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr17:63397600-63399000	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr17:63397600-63399000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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