Variant report

Variant	rs7762218
Chromosome Location	chr6:55005808-55005809
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs3105260	1.00[EUR][1000 genomes]
rs57915824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58658626	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59536488	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59630560	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6923998	1.00[EUR][1000 genomes]
rs73434487	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438551	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438552	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438561	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7356813	1.00[EUR][1000 genomes]
rs7740224	1.00[EUR][1000 genomes]
rs7766442	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55005400-55009600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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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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