Variant report

Variant	rs16932806
Chromosome Location	chr9:116100368-116100369
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:116098488..116100894-chr9:116162238..116164965,2	MCF-7	breast:
2	chr9:116100085..116103833-chr9:116137751..116140667,4	MCF-7	breast:
3	chr9:116099899..116105558-chr9:116170913..116174361,7	MCF-7	breast:
4	chr9:116035986..116039204-chr9:116098421..116104240,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000148229	Chromatin interaction
ENSG00000176386	Chromatin interaction
ENSG00000157653	Chromatin interaction
ENSG00000119431	Chromatin interaction
ENSG00000148218	Chromatin interaction
ENSG00000136875	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10817477	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981711	1.00[CEU][hapmap];0.83[CHB][hapmap];0.85[EUR][1000 genomes]
rs10981713	1.00[CEU][hapmap]
rs10981714	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10981718	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10981719	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10981721	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10981725	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10981734	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10981736	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10981754	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12350131	0.85[ASN][1000 genomes]
rs12684385	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12982	0.82[CEU][hapmap]
rs13289574	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16926630	0.82[CEU][hapmap]
rs16930959	1.00[CEU][hapmap]
rs16932083	0.96[EUR][1000 genomes]
rs16932730	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2296074	1.00[ASW][hapmap]
rs2296075	1.00[ASW][hapmap];1.00[CEU][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2296076	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2418249	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MKK][hapmap];0.92[TSI][hapmap];0.94[EUR][1000 genomes]
rs28480972	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34289746	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34294772	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34429100	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34749539	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35275471	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35772163	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35852964	0.89[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35860025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35915957	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3810915	1.00[ASW][hapmap];1.00[CEU][hapmap]
rs3810920	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4641140	1.00[CEU][hapmap]
rs59841233	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61161242	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71503561	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7850003	0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530949	chr9:115821128-116487796	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1042663	chr9:115920158-116167140	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv893744	chr9:115934852-116170227	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer 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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs16932806	WDR31	cis	Esophagus Mucosa	GTEx
rs16932806	WDR31	cis	lymphoblastoid	seeQTL

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116073800-116101600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr9:116077400-116101400	Weak transcription	Brain Germinal Matrix	brain
3	chr9:116077400-116101600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:116077800-116101200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr9:116080800-116101400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr9:116080800-116101600	Weak transcription	Fetal Brain Male	brain
7	chr9:116081000-116101600	Weak transcription	Pancreas	Pancrea
8	chr9:116082200-116101600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr9:116082600-116101400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr9:116082800-116101400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr9:116082800-116101600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:116082800-116101600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr9:116082800-116101600	Weak transcription	Brain Substantia Nigra	brain
14	chr9:116082800-116101600	Weak transcription	Fetal Kidney	kidney
15	chr9:116082800-116101600	Weak transcription	Fetal Muscle Trunk	muscle
16	chr9:116082800-116102000	Weak transcription	Aorta	Aorta
17	chr9:116083000-116101400	Weak transcription	Brain Cingulate Gyrus	brain
18	chr9:116083800-116101200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr9:116083800-116101200	Weak transcription	Colon Smooth Muscle	Colon
20	chr9:116083800-116101400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr9:116083800-116101600	Weak transcription	Right Ventricle	heart
22	chr9:116084000-116101400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:116084200-116101200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr9:116084200-116101400	Weak transcription	Liver	Liver
25	chr9:116084200-116101400	Weak transcription	Brain Anterior Caudate	brain
26	chr9:116084200-116101400	Weak transcription	Fetal Stomach	stomach
27	chr9:116084200-116101600	Weak transcription	Fetal Muscle Leg	muscle
28	chr9:116085400-116101400	Weak transcription	Adipose Nuclei	Adipose
29	chr9:116085400-116101400	Weak transcription	Fetal Lung	lung
30	chr9:116085400-116101600	Weak transcription	Brain Angular Gyrus	brain
31	chr9:116085600-116101200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr9:116091400-116101400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr9:116092000-116101400	Weak transcription	Small Intestine	intestine
34	chr9:116093000-116101400	Weak transcription	Fetal Intestine Small	intestine
35	chr9:116093000-116101800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr9:116093600-116101200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr9:116094400-116101200	Weak transcription	Left Ventricle	heart
38	chr9:116094400-116101400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr9:116094400-116101600	Weak transcription	Ovary	ovary
40	chr9:116095000-116101600	Weak transcription	Duodenum Mucosa	Duodenum
41	chr9:116098400-116101400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
42	chr9:116098400-116101400	Weak transcription	NHDF-Ad	bronchial
43	chr9:116099400-116101400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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