Variant report

Variant	rs1483075
Chromosome Location	chr7:49946838-49946839
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10237792	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10249896	0.93[YRI][hapmap];1.00[AMR][1000 genomes]
rs12111650	1.00[YRI][hapmap]
rs1483081	0.83[YRI][hapmap]
rs1483082	0.91[YRI][hapmap]
rs1532990	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1580402	0.92[YRI][hapmap]
rs1960762	0.91[YRI][hapmap]
rs2128663	1.00[YRI][hapmap]
rs2128940	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28887600	1.00[YRI][hapmap]
rs3807318	0.82[YRI][hapmap]
rs503212	0.82[AFR][1000 genomes]
rs523562	0.82[AFR][1000 genomes]
rs55803220	1.00[AMR][1000 genomes]
rs581181	0.82[AFR][1000 genomes]
rs624007	0.82[AFR][1000 genomes]
rs655184	0.83[AFR][1000 genomes]
rs6583418	0.82[YRI][hapmap]
rs6959913	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73336269	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73347089	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73349124	1.00[AMR][1000 genomes]
rs9886120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464444	chr7:49671882-50454736	Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv606897	chr7:49671883-50454736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv498090	chr7:49708644-50427714	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1020869	chr7:49712860-50457544	Enhancers Active TSS Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr7:49946600-49949000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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