Variant report

Variant	rs2733135
Chromosome Location	chr18:28354062-28354063
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs1943532	1.00[ASN][1000 genomes]
rs2591101	0.82[AFR][1000 genomes]
rs2591122	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2850267	0.81[AMR][1000 genomes]
rs28510557	1.00[ASN][1000 genomes]
rs3898132	1.00[ASN][1000 genomes]
rs4598986	0.98[ASN][1000 genomes]
rs4799299	1.00[ASN][1000 genomes]
rs56027591	1.00[ASN][1000 genomes]
rs62086430	0.99[ASN][1000 genomes]
rs73952509	1.00[ASN][1000 genomes]
rs9635999	0.98[ASN][1000 genomes]
rs9947312	0.99[ASN][1000 genomes]
rs9962487	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428675	chr18:28278505-28444515	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv909514	chr18:28321803-28420334	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28349200-28354600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr18:28353400-28355800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr18:28353800-28360800	Weak transcription	H1 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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