Variant report

Variant	rs12767557
Chromosome Location	chr10:22791665-22791666
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11599280	0.86[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs12221321	1.00[AFR][1000 genomes];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12770182	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35354362	0.82[ASN][1000 genomes]
rs4590763	0.84[ASW][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.94[JPT][hapmap];0.99[ASN][1000 genomes]
rs61847436	0.91[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs7092910	0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22765800-22806600	Weak transcription	Right Atrium	heart
2	chr10:22790600-22793000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr10:22790600-22794600	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr10:22790600-22794800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:22790800-22794800	Weak transcription	Primary T cells from cord blood	blood
6	chr10:22791200-22792400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr10:22791600-22791800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:22791600-22795200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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