Variant report

Variant	rs10082382
Chromosome Location	chr10:23294099-23294100
allele	A/G
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:15)

rs_ID	r²[population]
rs10741013	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10741014	0.83[ASN][1000 genomes]
rs10764370	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10764372	0.80[ASN][1000 genomes]
rs10828391	0.88[ASN][1000 genomes]
rs10828393	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1170665	0.80[ASN][1000 genomes]
rs1300432	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4748831	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4748832	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7070539	0.83[ASN][1000 genomes]
rs7075999	0.81[ASN][1000 genomes]
rs7079729	0.81[ASN][1000 genomes]
rs7080677	0.81[ASN][1000 genomes]
rs7909174	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23282800-23294200	Weak transcription	Pancreas	Pancrea
2	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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