Variant report

Variant	rs11236932
Chromosome Location	chr11:76486944-76486945
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10459050	0.97[ASN][1000 genomes]
rs10899284	0.87[ASN][1000 genomes]
rs11236925	1.00[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs11236933	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11236934	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11236938	1.00[CHB][hapmap];0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs1149618	1.00[YRI][hapmap]
rs3740771	1.00[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3740772	1.00[CHB][hapmap];0.88[JPT][hapmap];0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3758712	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs55738350	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs56941231	0.89[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs58039301	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs61302956	0.87[ASN][1000 genomes]
rs73503652	0.97[ASN][1000 genomes]
rs7925095	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7925436	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7925977	0.95[ASN][1000 genomes]
rs7941392	0.89[AMR][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76481000-76487800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:76482800-76492400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr11:76483600-76487600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr11:76484600-76487400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:76485600-76487600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:76485600-76489800	Weak transcription	Esophagus	oesophagus
7	chr11:76485600-76492200	Weak transcription	Ovary	ovary
8	chr11:76486000-76492200	Weak transcription	Liver	Liver
9	chr11:76486200-76488400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr11:76486400-76491600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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