Variant report

Variant	rs2332056
Chromosome Location	chr3:121598297-121598298
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10934568	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs12489511	0.81[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.90[JPT][hapmap];0.84[TSI][hapmap];0.82[ASN][1000 genomes]
rs12490565	0.87[ASW][hapmap];1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12695420	0.80[AMR][1000 genomes]
rs17849995	0.82[ASN][1000 genomes]
rs1919552	0.95[CEU][hapmap];0.82[CHB][hapmap];0.88[GIH][hapmap]
rs1919557	0.95[CEU][hapmap];0.82[CHB][hapmap];0.88[GIH][hapmap]
rs2001391	0.95[CEU][hapmap];0.82[CHB][hapmap];0.88[GIH][hapmap]
rs2141614	1.00[JPT][hapmap]
rs2700424	0.90[CHB][hapmap];0.81[JPT][hapmap];0.82[AMR][1000 genomes]
rs34227248	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34920680	0.89[ASN][1000 genomes]
rs34980632	0.82[ASN][1000 genomes]
rs3817599	0.86[GIH][hapmap];0.90[JPT][hapmap];0.83[TSI][hapmap];0.82[AMR][1000 genomes]
rs4676751	0.82[ASN][1000 genomes]
rs4676754	0.86[ASN][1000 genomes]
rs6438660	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap]
rs6438661	0.81[ASN][1000 genomes]
rs6438689	0.82[AMR][1000 genomes]
rs6770115	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6770719	0.87[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.89[ASN][1000 genomes]
rs6771716	0.89[ASN][1000 genomes]
rs6776703	0.82[ASN][1000 genomes]
rs6780559	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6791510	0.81[ASN][1000 genomes]
rs6807711	0.95[CEU][hapmap];0.82[CHB][hapmap];0.84[GIH][hapmap]
rs73181839	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7646346	0.95[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.95[ASN][1000 genomes]
rs7646585	0.95[CEU][hapmap];0.82[CHB][hapmap]
rs7652239	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs953730	0.82[GIH][hapmap]
rs9681209	1.00[CEU][hapmap];0.82[CHB][hapmap];0.90[JPT][hapmap]
rs9812411	0.90[CEU][hapmap];0.82[CHB][hapmap];0.88[GIH][hapmap]
rs9815649	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs9828757	0.82[AMR][1000 genomes]
rs9843053	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432480	chr3:121355723-121629928	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432482	chr3:121364236-121629634	Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv432481	chr3:121364236-121637178	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	nsv516233	chr3:121419301-121670405	Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
5	nsv877383	chr3:121465220-121650736	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
6	nsv432483	chr3:121488995-121629634	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	esv33139	chr3:121500400-122091831	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs2332056	EAF2	Cis_1M	lymphoblastoid	RTeQTL
rs2332056	HCLS1	Cis_1M	lymphoblastoid	RTeQTL
rs2332056	SLC15A2	cis	parietal	SCAN
rs2332056	SLC15A2	cis	cerebellum	SCAN
rs2332056	ADPRH	cis	parietal	SCAN
rs2332056	MUC13	cis	cerebellum	SCAN

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121554800-121604000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:121555800-121615600	Weak transcription	Primary T cells from cord blood	blood
3	chr3:121559200-121613200	Weak transcription	Brain Angular Gyrus	brain
4	chr3:121571400-121604200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr3:121583400-121612400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr3:121585000-121607600	Weak transcription	Aorta	Aorta
7	chr3:121585000-121613200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr3:121589600-121602600	Weak transcription	Fetal Lung	lung
9	chr3:121591400-121601600	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr3:121592800-121646800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr3:121593000-121604000	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr3:121593000-121615400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr3:121593000-121632400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr3:121593800-121602000	Weak transcription	Primary hematopoietic stem cells	blood
15	chr3:121594400-121598600	Weak transcription	GM12878-XiMat	blood
16	chr3:121595200-121598800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr3:121597200-121598800	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr3:121597400-121605600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr3:121597600-121600000	Strong transcription	Primary B cells from cord blood	blood
20	chr3:121597800-121598400	Weak transcription	Primary B cells from peripheral blood	blood
21	chr3:121598000-121598400	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr3:121598200-121601200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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