Variant report

Variant	rs729043
Chromosome Location	chr10:91568997-91568998
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10881624	0.84[ASN][1000 genomes]
rs10881641	0.89[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10881680	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11185822	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs11185823	0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11185824	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs11185827	0.84[ASN][1000 genomes]
rs11185828	0.84[ASN][1000 genomes]
rs11185840	0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11185843	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11185844	0.84[ASN][1000 genomes]
rs11185848	0.89[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11185849	0.88[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs12254780	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1324701	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1998646	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2104370	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58526788	0.98[ASN][1000 genomes]
rs735934	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046241	chr10:91478562-91614437	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv869080	chr10:91498641-91712834	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv1036581	chr10:91526705-91691536	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv947684	chr10:91566760-91569416	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
5	nsv1043571	chr10:91568555-92036154	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91566000-91569200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr10:91568600-91569000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr10:91568600-91569000	Enhancers	GM12878-XiMat	blood
4	chr10:91568600-91569200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr10:91568800-91569000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr10:91568800-91569000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr10:91568800-91569800	Enhancers	Cortex derived primary cultured neurospheres	brain

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

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