Variant report

Variant	rs35426056
Chromosome Location	chr6:81413424-81413425
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:81412447..81415147-chr6:82462041..82464477,2	K562	blood:

Variant related genes	Relation type
ENSG00000112773	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10485283	0.83[EUR][1000 genomes]
rs10485286	0.86[EUR][1000 genomes]
rs12661465	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12662185	0.83[EUR][1000 genomes]
rs12662485	0.83[EUR][1000 genomes]
rs12663226	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12663298	0.83[EUR][1000 genomes]
rs12663591	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13197256	0.86[EUR][1000 genomes]
rs13198210	0.83[EUR][1000 genomes]
rs13198536	0.83[EUR][1000 genomes]
rs13211723	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13212232	0.83[EUR][1000 genomes]
rs13212944	0.83[EUR][1000 genomes]
rs13213267	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1454450	0.82[ASN][1000 genomes]
rs1598169	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16892136	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16892139	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16892242	0.86[EUR][1000 genomes]
rs16892247	0.83[EUR][1000 genomes]
rs16892249	0.83[EUR][1000 genomes]
rs34394883	0.83[EUR][1000 genomes]
rs34504200	0.83[EUR][1000 genomes]
rs34570868	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34687169	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34969790	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35052062	0.83[EUR][1000 genomes]
rs35090599	0.86[EUR][1000 genomes]
rs35237645	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35251642	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35489422	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36044530	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71565102	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs71566904	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs71566906	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs71566907	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73465800	0.83[EUR][1000 genomes]
rs73468242	0.83[EUR][1000 genomes]
rs73748847	0.83[EUR][1000 genomes]
rs997835	0.83[EUR][1000 genomes]
rs998078	0.83[EUR][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	nsv531333	chr6:81042427-81836484	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1019670	chr6:81086504-81569984	ZNF genes & repeats Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	nsv604085	chr6:81297890-81439973	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv886315	chr6:81352515-81946866	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv886316	chr6:81390313-81554464	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 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	chr6:81412600-81413600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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