Variant report

Variant	rs4365740
Chromosome Location	chr4:124458090-124458091
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs12503335	0.95[ASN][1000 genomes]
rs1452732	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17752451	0.84[ASN][1000 genomes]
rs17809071	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1993190	0.86[ASN][1000 genomes]
rs2014110	0.83[ASN][1000 genomes]
rs2553360	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2553363	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2553372	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2553373	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2553374	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2553375	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2553377	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2589836	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2589865	0.84[ASN][1000 genomes]
rs4254791	0.83[ASN][1000 genomes]
rs4254792	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4286523	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4377602	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4400004	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4596251	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4833280	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4833282	0.84[ASN][1000 genomes]
rs4833931	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6534412	0.86[ASN][1000 genomes]
rs6534414	0.87[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs6813552	0.87[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs6832678	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs6838729	0.84[ASN][1000 genomes]
rs766162	0.82[ASN][1000 genomes]
rs7664219	0.82[ASN][1000 genomes]
rs7694928	0.85[ASN][1000 genomes]
rs979998	0.86[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	nsv1006945	chr4:124206328-124503863	Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv537240	chr4:124206328-124503863	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	esv34581	chr4:124271321-125247395	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv879871	chr4:124437842-124527958	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv879872	chr4:124441989-124527958	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 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	chr4:124428000-124471800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr4:124451000-124466400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:124451200-124464800	Weak transcription	HepG2	liver
4	chr4:124452200-124460000	Weak transcription	Liver	Liver
5	chr4:124453200-124460200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:124453200-124467200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr4:124456800-124458400	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr4:124457400-124458200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr4:124457600-124458600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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