Variant report

Variant	rs7082307
Chromosome Location	chr10:4167639-4167640
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10751960	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10751961	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10904197	0.87[ASN][1000 genomes]
rs1885475	0.87[ASN][1000 genomes]
rs2146058	0.80[ASN][1000 genomes]
rs6601814	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6601815	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs7069371	0.86[AMR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051297	chr10:3908706-4277678	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv831772	chr10:4039292-4212218	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4163000-4173400	Weak transcription	NHLF	lung
2	chr10:4164000-4170000	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr10:4164400-4169600	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr10:4164600-4169600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr10:4167200-4174200	Weak transcription	Pancreas	Pancrea
6	chr10:4167400-4169400	Weak transcription	Primary B cells from peripheral blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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