Variant report

Variant	rs66732283
Chromosome Location	chr15:53206382-53206383
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs16965313	0.90[EUR][1000 genomes]
rs17543902	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1899737	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28758654	0.90[EUR][1000 genomes]
rs56876630	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61262002	0.90[EUR][1000 genomes]
rs61592493	0.87[EUR][1000 genomes]
rs7163077	0.90[EUR][1000 genomes]
rs7163093	0.90[EUR][1000 genomes]
rs7169953	0.88[EUR][1000 genomes]
rs72742108	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72742109	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72742144	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72742157	0.88[AFR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53204200-53207400	Weak transcription	Pancreas	Pancrea
2	chr15:53205000-53206600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr15:53205200-53207600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr15:53205200-53207600	Weak transcription	iPS-18 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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