Variant report

Variant	rs10826317
Chromosome Location	chr10:61331453-61331454
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11006585	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11006600	0.96[ASN][1000 genomes]
rs11006609	0.89[ASN][1000 genomes]
rs12415404	0.96[ASN][1000 genomes]
rs12416613	0.96[ASN][1000 genomes]
rs16913829	0.96[ASN][1000 genomes]
rs2393559	0.94[ASN][1000 genomes]
rs35710625	0.96[ASN][1000 genomes]
rs7918255	0.94[ASN][1000 genomes]
rs7918394	0.93[ASN][1000 genomes]
rs7919042	0.94[ASN][1000 genomes]
rs7922399	0.94[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	esv2757394	chr10:61324135-61333139	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv2759762	chr10:61324135-61333139	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61331400-61336200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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