Variant report

Variant	rs2820878
Chromosome Location	chr1:216900811-216900812
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12059942	0.93[EUR][1000 genomes]
rs1339350	0.84[ASN][1000 genomes]
rs1339357	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2789730	0.86[CEU][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2789732	0.82[ASN][1000 genomes]
rs2789733	0.85[ASN][1000 genomes]
rs2820875	0.85[ASN][1000 genomes]
rs2820876	0.85[ASN][1000 genomes]
rs2999504	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:216897400-216901400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:216897400-216958600	Weak transcription	Pancreas	Pancrea

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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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