Variant report

Variant	rs1927855
Chromosome Location	chr13:54098398-54098399
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54094400-54098800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr13:54094600-54099000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:54094600-54099000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr13:54094800-54098600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr13:54094800-54098800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr13:54094800-54099000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr13:54094800-54099200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr13:54095000-54098600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr13:54097400-54102400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr13:54097800-54100600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

Quick Search:

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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