Variant report

Variant	rs73471188
Chromosome Location	chr18:39992005-39992006
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs16960221	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16976021	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2060137	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56318343	1.00[EUR][1000 genomes]
rs59046070	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59980203	1.00[EUR][1000 genomes]
rs61067214	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61641935	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7229024	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73471193	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73951515	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8087636	1.00[EUR][1000 genomes]

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	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1059409	chr18:39711099-40139446	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv909572	chr18:39938510-40064000	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	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	chr18:39989400-39993400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:39989400-39993600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:39989400-39993600	Weak transcription	iPS DF 19.11 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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