Variant report

Variant	rs4944108
Chromosome Location	chr11:76120138-76120139
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11236742	0.86[CEU][hapmap];0.81[JPT][hapmap];0.84[EUR][1000 genomes]
rs4944107	0.81[EUR][1000 genomes]
rs4945080	0.81[EUR][1000 genomes]
rs4945083	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4945084	0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6592633	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7115322	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7129437	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7928709	0.84[CEU][hapmap]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76097200-76122000	Weak transcription	Fetal Stomach	stomach
2	chr11:76118200-76120200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr11:76118800-76120400	Enhancers	Fetal Kidney	kidney
4	chr11:76119200-76120200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr11:76119200-76120200	Enhancers	HUVEC	blood vessel
6	chr11:76119200-76120800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:76119600-76120200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr11:76119600-76120200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:76119600-76120200	Enhancers	Fetal Thymus	thymus

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Input of quick search could be:

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

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