Variant report

Variant	rs4082827
Chromosome Location	chr4:74831180-74831181
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:74829266..74831770-chr4:74833383..74836312,2	K562	blood:

Extended variants
information (count: 66 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10007249	0.93[EUR][1000 genomes]
rs10017182	0.84[ASN][1000 genomes]
rs10033521	0.84[ASN][1000 genomes]
rs10518117	0.85[CEU][hapmap];0.92[GIH][hapmap];0.86[EUR][1000 genomes]
rs10938105	0.82[ASN][1000 genomes]
rs11508014	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11574452	0.85[CEU][hapmap]
rs12108606	0.83[EUR][1000 genomes]
rs12498174	0.82[ASN][1000 genomes]
rs13120504	0.82[ASN][1000 genomes]
rs13128887	0.82[ASN][1000 genomes]
rs1429637	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1435520	0.85[CEU][hapmap];0.85[AMR][1000 genomes]
rs149611	0.89[EUR][1000 genomes]
rs1511815	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs16845091	0.86[EUR][1000 genomes]
rs16850160	0.86[EUR][1000 genomes]
rs16850178	0.86[EUR][1000 genomes]
rs1951233	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs1957069	0.85[CEU][hapmap];0.92[GIH][hapmap]
rs2180883	0.84[GIH][hapmap]
rs2195543	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2367427	0.86[EUR][1000 genomes]
rs2367443	0.82[ASN][1000 genomes]
rs2564596	0.80[ASN][1000 genomes]
rs3111693	0.84[GIH][hapmap]
rs3114083	0.86[ASN][1000 genomes]
rs352036	0.89[EUR][1000 genomes]
rs353028	0.89[EUR][1000 genomes]
rs353029	0.89[EUR][1000 genomes]
rs353031	0.93[EUR][1000 genomes]
rs353032	0.83[EUR][1000 genomes]
rs353034	0.93[EUR][1000 genomes]
rs353039	0.93[EUR][1000 genomes]
rs353040	0.93[EUR][1000 genomes]
rs353042	0.85[CEU][hapmap];1.00[TSI][hapmap]
rs3756074	0.85[CEU][hapmap]
rs3906613	0.84[ASN][1000 genomes]
rs4399951	0.82[ASN][1000 genomes]
rs4694657	0.81[ASN][1000 genomes]
rs4694658	0.82[ASN][1000 genomes]
rs499141	0.93[EUR][1000 genomes]
rs529312	0.93[EUR][1000 genomes]
rs57274239	0.89[EUR][1000 genomes]
rs58324794	0.83[EUR][1000 genomes]
rs58463118	0.86[EUR][1000 genomes]
rs585778	0.93[EUR][1000 genomes]
rs58610473	0.83[EUR][1000 genomes]
rs60775930	0.86[EUR][1000 genomes]
rs629315	0.93[EUR][1000 genomes]
rs671253	0.86[EUR][1000 genomes]
rs6813021	0.81[ASN][1000 genomes]
rs6813952	0.81[CHB][hapmap];0.90[CHD][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6819077	0.82[ASN][1000 genomes]
rs6822890	0.82[ASN][1000 genomes]
rs72855280	0.92[ASN][1000 genomes]
rs7666671	0.93[EUR][1000 genomes]
rs8180167	0.84[ASN][1000 genomes]
rs9291189	0.84[ASN][1000 genomes]
rs938094	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv1004768	chr4:74774372-75109579	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv1006218	chr4:74782324-75105424	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv1006029	chr4:74793922-74986664	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4082827	DDX43	trans	lymphoblastoid	seeQTL

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74810200-74844600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:74830400-74831200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr4:74830600-74831200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:74830600-74831200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:74830600-74831200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:74830600-74831400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:74831000-74831200	Enhancers	Gastric	stomach

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