Variant report

Variant	rs35802624
Chromosome Location	chr6:12505074-12505075
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10807283	0.92[ASN][1000 genomes]
rs13211009	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13214464	0.89[EUR][1000 genomes]
rs13217076	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1413513	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1999622	0.92[ASN][1000 genomes]
rs2876273	0.92[ASN][1000 genomes]
rs4714632	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7743158	0.92[ASN][1000 genomes]
rs7753779	0.94[ASN][1000 genomes]
rs9349245	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9369371	0.91[ASN][1000 genomes]
rs9381221	0.96[ASN][1000 genomes]
rs9381224	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9471883	0.91[ASN][1000 genomes]
rs9471890	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12492000-12506000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:12502800-12505600	Weak transcription	Brain Germinal Matrix	brain

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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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