Variant report

Variant	rs73918008
Chromosome Location	chr2:21194111-21194112
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs56080455	0.85[AFR][1000 genomes]
rs56164002	0.83[AMR][1000 genomes]
rs61079625	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73918003	0.88[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73918005	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73918011	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73921326	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73921332	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73921339	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73921340	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7594128	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21189600-21195000	Weak transcription	Aorta	Aorta
2	chr2:21192000-21194400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr2:21194000-21195000	Weak transcription	Stomach Smooth Muscle	stomach

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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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