Variant report

Variant	rs11187741
Chromosome Location	chr10:95725386-95725387
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10882378	0.89[ASN][1000 genomes]
rs10882379	0.89[ASN][1000 genomes]
rs11187760	0.84[ASN][1000 genomes]
rs11187765	0.80[ASN][1000 genomes]
rs11187767	0.80[ASN][1000 genomes]
rs11599672	0.88[ASN][1000 genomes]
rs12573786	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3814689	0.85[ASN][1000 genomes]
rs61866000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7073291	0.89[ASN][1000 genomes]
rs7094594	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95707800-95725600	Weak transcription	Ovary	ovary
2	chr10:95712200-95725600	Weak transcription	Spleen	Spleen
3	chr10:95719000-95728400	Weak transcription	Fetal Intestine Small	intestine
4	chr10:95719600-95728400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:95721000-95727400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr10:95723600-95728400	Weak transcription	Fetal Muscle Leg	muscle
7	chr10:95724800-95725800	Weak transcription	Right Atrium	heart

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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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