Variant report

Variant	rs35579427
Chromosome Location	chr1:217325278-217325279
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]
rs11576172	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11579927	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11586921	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12739810	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12749238	0.96[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12751962	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35478056	1.00[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs35963574	1.00[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs71643444	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71643445	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217318400-217325800	Weak transcription	Aorta	Aorta
2	chr1:217323400-217327000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:217324600-217326000	Enhancers	Fetal Stomach	stomach
4	chr1:217325200-217325400	Enhancers	Colon Smooth Muscle	Colon
5	chr1:217325200-217326000	Enhancers	Fetal Lung	lung
6	chr1:217325200-217327200	Enhancers	Fetal Heart	heart

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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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