Variant report

Variant	rs112744067
Chromosome Location	chr3:93509261-93509262
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3375759	chr3:93507123-93515343	Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
2	esv3370198	chr3:93509062-93519960	Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a
3	esv3438490	chr3:93509262-93519660	Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:93508000-93510200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr3:93508000-93510400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:93508200-93510200	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:93508200-93510200	Weak transcription	HUES64 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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