Variant report

Variant	rs11119711
Chromosome Location	chr1:211403550-211403551
allele	C/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:14)

rs_ID	r²[population]
rs10779551	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10863885	0.92[ASN][1000 genomes]
rs11119714	0.94[ASN][1000 genomes]
rs11119717	0.91[ASN][1000 genomes]
rs11119720	0.91[ASN][1000 genomes]
rs12032988	0.91[ASN][1000 genomes]
rs12041794	0.94[ASN][1000 genomes]
rs12042216	0.94[ASN][1000 genomes]
rs12046975	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12095365	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17017360	0.91[ASN][1000 genomes]
rs4540732	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59019096	0.92[ASN][1000 genomes]
rs9887769	0.93[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211397800-211405200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr1:211402200-211403600	Enhancers	Primary hematopoietic stem cells	blood
3	chr1:211402800-211403800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:211403200-211403800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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