Variant report

Variant	rs73497629
Chromosome Location	chr9:103450482-103450483
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs16919293	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16919321	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16919323	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1857630	0.88[EUR][1000 genomes]
rs2096355	0.88[EUR][1000 genomes]
rs2096356	0.88[EUR][1000 genomes]
rs60349573	0.88[EUR][1000 genomes]
rs6479021	0.88[EUR][1000 genomes]
rs7044571	0.88[EUR][1000 genomes]
rs73495750	0.88[EUR][1000 genomes]
rs73495767	0.88[EUR][1000 genomes]
rs73495775	0.88[EUR][1000 genomes]
rs73497610	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7850373	0.88[EUR][1000 genomes]
rs7853484	0.88[EUR][1000 genomes]
rs7859563	0.88[EUR][1000 genomes]
rs7870742	0.88[EUR][1000 genomes]
rs7874312	0.88[EUR][1000 genomes]
rs7874610	0.88[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103450000-103472400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:103450400-103452800	Weak transcription	H9 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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