Variant report

Variant	rs6660266
Chromosome Location	chr1:213677590-213677591
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1025765	0.94[ASN][1000 genomes]
rs105959	0.91[ASN][1000 genomes]
rs11120146	0.93[ASN][1000 genomes]
rs11120147	0.94[ASN][1000 genomes]
rs2165129	0.96[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2165130	0.93[ASN][1000 genomes]
rs2165133	0.94[ASN][1000 genomes]
rs2173482	0.93[ASN][1000 genomes]
rs320374	0.93[ASN][1000 genomes]
rs451083	0.94[ASN][1000 genomes]
rs893664	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832525	chr1:213580476-213782815	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213673000-213678200	Weak transcription	Pancreas	Pancrea

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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