Variant report

Variant	rs17007598
Chromosome Location	chr1:220562855-220562856
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs17007609	1.00[EUR][1000 genomes]
rs57124487	1.00[EUR][1000 genomes]
rs58541644	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73092212	1.00[EUR][1000 genomes]
rs73104963	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73104966	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73104972	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73104982	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73104996	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73104999	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7529207	0.83[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	chr1:220562600-220563800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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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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