Variant report

Variant	rs2364844
Chromosome Location	chr10:23294664-23294665
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10508656	0.86[ASN][1000 genomes]
rs10828389	0.87[ASN][1000 genomes]
rs10828390	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10828392	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11013225	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11013232	0.93[EUR][1000 genomes]
rs12359749	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1987026	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35373354	0.86[ASN][1000 genomes]
rs55727318	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7077613	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7083053	0.87[ASN][1000 genomes]
rs7083069	0.87[ASN][1000 genomes]
rs7084413	0.86[ASN][1000 genomes]
rs7895048	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7907625	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7911289	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23291200-23295000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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