Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs13437579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28444386	1.00[ASN][1000 genomes]
rs28461820	1.00[ASN][1000 genomes]
rs34060138	1.00[ASN][1000 genomes]
rs388183	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs446711	1.00[ASN][1000 genomes]
rs724700	1.00[ASN][1000 genomes]
rs9464728	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9464729	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9464730	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9464731	1.00[ASN][1000 genomes]
rs9464732	1.00[ASN][1000 genomes]
rs9464733	1.00[ASN][1000 genomes]
rs9464734	1.00[ASN][1000 genomes]
rs9476669	1.00[ASN][1000 genomes]
rs9476674	1.00[ASN][1000 genomes]
rs9476675	1.00[ASN][1000 genomes]
rs9476676	1.00[ASN][1000 genomes]
rs9476678	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9476679	1.00[ASN][1000 genomes]
rs9476680	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9476682	1.00[ASN][1000 genomes]
rs9476683	1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9476684	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9476685	1.00[ASN][1000 genomes]
rs9476686	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031668	chr6:14774036-15044308	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv538138	chr6:14774036-15044308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1017572	chr6:14830510-14906933	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14890800-14897000	Weak transcription	Stomach Mucosa	stomach
2	chr6:14890800-14897800	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr6:14893800-14894800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
4	chr6:14893800-14894800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
5	chr6:14893800-14896800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr6:14894000-14894800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr6:14894000-14895000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
8	chr6:14894400-14912400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:14894400-14915800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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