Variant report

Variant	rs7802895
Chromosome Location	chr7:127070485-127070486
allele	A/G
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]
rs10230771	0.86[EUR][1000 genomes]
rs10279764	0.86[EUR][1000 genomes]
rs10808228	0.86[EUR][1000 genomes]
rs10954150	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11772370	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12706789	0.86[EUR][1000 genomes]
rs12706790	0.86[EUR][1000 genomes]
rs1419404	0.86[EUR][1000 genomes]
rs1833067	0.86[EUR][1000 genomes]
rs2157749	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4731360	0.86[EUR][1000 genomes]
rs4731361	0.86[EUR][1000 genomes]
rs4731362	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7808943	0.86[EUR][1000 genomes]
rs7809156	0.86[EUR][1000 genomes]
rs7809187	0.86[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127070400-127072400	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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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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