Variant report

Variant	rs17041676
Chromosome Location	chr2:21194905-21194906
allele	A/G
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]
rs10495715	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs12713558	1.00[ASW][hapmap];0.93[MKK][hapmap];0.80[YRI][hapmap]
rs12720792	1.00[ASW][hapmap];0.90[MKK][hapmap]
rs12720847	1.00[ASW][hapmap];0.93[MKK][hapmap];1.00[YRI][hapmap]
rs17041647	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17041656	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17041688	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17041694	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4665645	0.86[AMR][1000 genomes]
rs73918013	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7558478	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][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	chr2:21194000-21195000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr2:21194400-21195600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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