Variant report

Variant	rs34428863
Chromosome Location	chr6:166605770-166605771
allele	C/T
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]
rs13199606	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13215259	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3099271	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3099313	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3127360	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34188346	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34475811	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34651251	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34732671	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35245884	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36133170	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57772015	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs71571437	0.87[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:166587800-166608400	Weak transcription	Pancreas	Pancrea
2	chr6:166605600-166609000	Weak transcription	Spleen	Spleen

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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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