Variant report

Variant	rs3782214
Chromosome Location	chr12:117764640-117764641
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11068418	1.00[TSI][hapmap]
rs11068443	1.00[TSI][hapmap]
rs11068450	0.93[GIH][hapmap]
rs16947485	1.00[JPT][hapmap];0.90[YRI][hapmap];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2293044	1.00[TSI][hapmap]
rs57719099	1.00[EUR][1000 genomes]
rs58264841	1.00[EUR][1000 genomes]
rs58471203	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59689997	1.00[EUR][1000 genomes]
rs60330472	1.00[EUR][1000 genomes]
rs60346882	1.00[EUR][1000 genomes]
rs7306231	1.00[AMR][1000 genomes]
rs9658259	1.00[EUR][1000 genomes]
rs9658268	1.00[JPT][hapmap]
rs9658280	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9658284	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9658317	1.00[AMR][1000 genomes]
rs9658325	1.00[AMR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117728000-117771200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr12:117739800-117771400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr12:117749400-117770800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:117762200-117771200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:117763400-117766000	Weak transcription	NHEK	skin
6	chr12:117764200-117765600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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