Variant report

Variant	rs570238193
Chromosome Location	chr5:116694489-116694490
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882755	chr5:116647725-116748877	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv7238	chr5:116694326-116695085	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
3	esv3469781	chr5:116694376-116694946	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
4	esv3324676	chr5:116694429-116694967	Weak transcription	n/a	n/a	inside rSNPs	n/a
5	esv3528797	chr5:116694431-116694907	Weak transcription	n/a	n/a	inside rSNPs	n/a
6	esv3469780	chr5:116694433-116694913	Weak transcription	n/a	n/a	inside rSNPs	n/a
7	esv3469782	chr5:116694450-116694860	Weak transcription	n/a	n/a	inside rSNPs	n/a
8	esv3427677	chr5:116694460-116694906	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116687200-116697200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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