Variant report

Variant	rs13390311
Chromosome Location	chr2:191246782-191246783
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10170897	0.98[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10190016	0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.93[ASN][1000 genomes]
rs10202825	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.93[ASN][1000 genomes]
rs10208045	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13409203	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16832573	0.90[CHB][hapmap]
rs34121676	0.81[ASN][1000 genomes]
rs3811610	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs73048070	0.97[ASN][1000 genomes]
rs73050047	0.93[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191231800-191247800	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:191244600-191246800	Enhancers	K562	blood
3	chr2:191244600-191248800	Weak transcription	Gastric	stomach
4	chr2:191244800-191246800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr2:191245400-191247000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr2:191245800-191247000	Enhancers	Brain Cingulate Gyrus	brain
7	chr2:191246400-191247400	Weak transcription	Fetal Lung	lung

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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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