Variant report

Variant	rs7747706
Chromosome Location	chr6:54899291-54899292
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs13191783	1.00[EUR][1000 genomes]
rs13192880	0.87[EUR][1000 genomes]
rs13196537	0.87[EUR][1000 genomes]
rs13199854	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs13200567	1.00[EUR][1000 genomes]
rs13201525	1.00[EUR][1000 genomes]
rs13202991	1.00[EUR][1000 genomes]
rs13204748	1.00[EUR][1000 genomes]
rs13207382	1.00[EUR][1000 genomes]
rs13208146	1.00[EUR][1000 genomes]
rs13210210	1.00[EUR][1000 genomes]
rs13211183	1.00[EUR][1000 genomes]
rs13218015	1.00[EUR][1000 genomes]
rs34015457	1.00[EUR][1000 genomes]
rs34187954	1.00[EUR][1000 genomes]
rs34202476	1.00[EUR][1000 genomes]
rs34267888	0.86[EUR][1000 genomes]
rs34321112	1.00[EUR][1000 genomes]
rs34327080	1.00[EUR][1000 genomes]
rs34491203	1.00[EUR][1000 genomes]
rs34602564	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34841798	1.00[EUR][1000 genomes]
rs34896294	1.00[EUR][1000 genomes]
rs34920015	1.00[EUR][1000 genomes]
rs34950463	1.00[EUR][1000 genomes]
rs35081106	1.00[EUR][1000 genomes]
rs35094736	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35124020	0.87[EUR][1000 genomes]
rs35253545	1.00[EUR][1000 genomes]
rs35326632	1.00[EUR][1000 genomes]
rs35729004	1.00[EUR][1000 genomes]
rs35908115	1.00[EUR][1000 genomes]
rs35925278	0.87[EUR][1000 genomes]
rs36030916	1.00[EUR][1000 genomes]
rs36062413	1.00[EUR][1000 genomes]
rs36115210	1.00[EUR][1000 genomes]
rs4524608	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71560876	1.00[EUR][1000 genomes]
rs71560878	1.00[EUR][1000 genomes]
rs71560879	1.00[EUR][1000 genomes]
rs71560885	1.00[EUR][1000 genomes]
rs71560887	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs71560895	1.00[EUR][1000 genomes]
rs71560900	0.86[EUR][1000 genomes]
rs71560901	0.86[EUR][1000 genomes]
rs7767204	1.00[EUR][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	esv3364886	chr6:54880042-54912395	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
2	esv3368520	chr6:54881042-54905736	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
3	nsv1033756	chr6:54881828-54944304	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv538225	chr6:54881828-54944304	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 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	chr6:54897800-54899600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr6:54897800-54900600	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr6:54897800-54900800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr6:54898000-54900800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:54898800-54900800	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr6:54899000-54900600	Enhancers	Primary hematopoietic stem cells	blood
7	chr6:54899000-54900600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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