Variant report

Variant	rs17021635
Chromosome Location	chr1:214106075-214106076
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11808079	0.82[ASW][hapmap];1.00[CHB][hapmap];0.95[MKK][hapmap];0.96[YRI][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12065591	1.00[ASN][1000 genomes]
rs17021519	1.00[ASN][1000 genomes]
rs17021657	1.00[ASN][1000 genomes]
rs17021658	0.88[ASW][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17021669	1.00[ASN][1000 genomes]
rs58653950	1.00[ASN][1000 genomes]
rs58802903	1.00[ASN][1000 genomes]
rs6656171	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6665854	1.00[ASN][1000 genomes]
rs73084466	1.00[ASN][1000 genomes]
rs73084470	1.00[ASN][1000 genomes]
rs74139070	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214104400-214109200	Enhancers	Fetal Heart	heart
2	chr1:214105200-214106600	Enhancers	Fetal Lung	lung
3	chr1:214105400-214107400	Weak transcription	Left Ventricle	heart
4	chr1:214105600-214107400	Weak transcription	Brain Hippocampus Middle	brain
5	chr1:214105800-214106600	Enhancers	Pancreas	Pancrea
6	chr1:214105800-214107800	Enhancers	Liver	Liver
7	chr1:214106000-214108400	Enhancers	Cortex derived primary cultured neurospheres	brain

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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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