Variant report

Variant	rs7585344
Chromosome Location	chr2:172992896-172992897
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10179179	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10187941	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10202930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13387007	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs13410748	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs9973462	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172991400-172993400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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