Variant report

Variant	rs4713784
Chromosome Location	chr6:34403234-34403235
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34202536..34205881-chr6:34403058..34404790,3	K562	blood:
2	chr6:34396044..34398676-chr6:34403106..34407156,3	K562	blood:
3	chr6:34203058..34205881-chr6:34403223..34405394,2	K562	blood:

Variant related genes	Relation type
ENSG00000137309	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12664001	0.90[AMR][1000 genomes]
rs12664016	0.81[AMR][1000 genomes]
rs12665397	0.88[AMR][1000 genomes]
rs1573905	1.00[CEU][hapmap]
rs16885998	1.00[CEU][hapmap];0.87[MEX][hapmap]
rs16889706	1.00[CEU][hapmap];0.87[MEX][hapmap];0.90[AMR][1000 genomes]
rs16889714	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2071928	1.00[CEU][hapmap]
rs28847046	0.81[AMR][1000 genomes]
rs3778077	1.00[CEU][hapmap];0.91[MEX][hapmap];0.83[AMR][1000 genomes]
rs3798562	1.00[CEU][hapmap];0.86[MEX][hapmap];0.83[AMR][1000 genomes]
rs3798564	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs3800476	0.89[AMR][1000 genomes]
rs3800477	0.89[AMR][1000 genomes]
rs4295465	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4711390	1.00[CEU][hapmap];0.87[MEX][hapmap]
rs4713766	1.00[CEU][hapmap]
rs4713774	1.00[CEU][hapmap];0.81[AMR][1000 genomes]
rs4713775	0.90[AMR][1000 genomes]
rs4713776	0.90[AMR][1000 genomes]
rs4713777	0.82[MEX][hapmap];0.87[AMR][1000 genomes]
rs4713780	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4713781	0.87[AMR][1000 genomes]
rs4713783	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4713786	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4713787	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4713789	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58648597	0.81[AMR][1000 genomes]
rs59310759	0.81[AMR][1000 genomes]
rs60100381	0.83[AMR][1000 genomes]
rs61582147	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6909732	1.00[CEU][hapmap]
rs6935129	0.89[AMR][1000 genomes]
rs9348940	0.87[AMR][1000 genomes]
rs9368815	0.81[AMR][1000 genomes]
rs9394200	1.00[CEU][hapmap]
rs9766229	0.87[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	nsv1022844	chr6:34317219-35060519	Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv538195	chr6:34317219-35060519	Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	esv2758046	chr6:34382492-34714677	Genic enhancers Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	esv2759418	chr6:34382492-34714677	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4713784	RPS10	cis	lymphoblastoid	seeQTL

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34394200-34409200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:34394400-34433200	Weak transcription	Right Atrium	heart

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