Variant report

Variant	rs8785
Chromosome Location	chr11:9468454-9468455
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 101 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs1020621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1020622	1.00[ASN][1000 genomes]
rs10743107	0.90[ASN][1000 genomes]
rs10770028	1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs10770029	0.89[ASN][1000 genomes]
rs10770032	1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10770033	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10770034	0.83[ASN][1000 genomes]
rs10770037	0.84[CEU][hapmap];0.91[MEX][hapmap]
rs10840228	1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10840234	1.00[CHB][hapmap];0.88[JPT][hapmap];0.86[ASN][1000 genomes]
rs10840235	0.84[CHD][hapmap];0.84[GIH][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs10840236	0.93[ASN][1000 genomes]
rs10840237	0.98[ASN][1000 genomes]
rs10840238	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10840241	0.87[ASN][1000 genomes]
rs10840243	0.96[CEU][hapmap];0.95[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10840244	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10840245	0.95[JPT][hapmap];0.84[MEX][hapmap];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10840247	0.85[ASN][1000 genomes]
rs10840249	0.81[ASN][1000 genomes]
rs10840253	0.85[JPT][hapmap]
rs11042328	1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11042329	1.00[CHB][hapmap];0.94[CHD][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs11042348	0.97[ASN][1000 genomes]
rs11042349	0.94[ASN][1000 genomes]
rs11042350	0.92[ASW][hapmap];1.00[CEU][hapmap];0.95[GIH][hapmap];0.95[MEX][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11042353	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11042355	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11042356	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11042366	0.85[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11042374	0.84[ASN][1000 genomes]
rs11042377	0.86[ASN][1000 genomes]
rs11042395	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs11826606	0.94[ASN][1000 genomes]
rs12225755	0.94[ASN][1000 genomes]
rs12271897	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12282176	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12296039	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12792161	0.85[ASN][1000 genomes]
rs12795344	0.86[ASW][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.89[ASN][1000 genomes]
rs12797567	0.97[ASN][1000 genomes]
rs12799672	0.87[ASN][1000 genomes]
rs12800802	0.99[ASN][1000 genomes]
rs12806418	0.85[ASN][1000 genomes]
rs1377667	0.82[ASN][1000 genomes]
rs1470896	0.82[ASN][1000 genomes]
rs1543	0.82[ASN][1000 genomes]
rs1968717	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2278900	0.95[JPT][hapmap];0.83[MEX][hapmap];0.85[ASN][1000 genomes]
rs2290423	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.96[MEX][hapmap];0.89[TSI][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2290424	0.95[JPT][hapmap];0.84[MEX][hapmap];0.81[ASN][1000 genomes]
rs2290425	0.95[JPT][hapmap];0.84[MEX][hapmap];0.82[ASN][1000 genomes]
rs35781320	0.97[ASN][1000 genomes]
rs3763873	0.92[CEU][hapmap];0.86[GIH][hapmap]
rs3763874	0.80[MEX][hapmap]
rs3763877	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs41369549	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];1.00[ASN][1000 genomes]
rs4625466	0.94[JPT][hapmap]
rs4810	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4910048	0.91[GIH][hapmap]
rs4910053	0.95[JPT][hapmap]
rs4910468	0.82[ASN][1000 genomes]
rs6486306	0.86[ASN][1000 genomes]
rs6486307	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6486359	1.00[ASN][1000 genomes]
rs6486361	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6486394	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs67548305	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs68060819	0.82[ASN][1000 genomes]
rs7102473	0.86[ASN][1000 genomes]
rs7103931	0.88[ASN][1000 genomes]
rs7104568	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];1.00[ASN][1000 genomes]
rs7114824	0.92[ASN][1000 genomes]
rs7115477	0.84[GIH][hapmap]
rs7122252	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7122499	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs723297	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs727405	0.92[CEU][hapmap];0.88[GIH][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs729313	0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs7395411	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7480643	0.82[GIH][hapmap]
rs7483667	0.84[ASN][1000 genomes]
rs7926589	0.96[CEU][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7927350	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7928823	0.85[ASN][1000 genomes]
rs7928945	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7932192	0.89[ASN][1000 genomes]
rs7933621	0.86[ASN][1000 genomes]
rs7939724	0.84[CEU][hapmap];0.92[MEX][hapmap]
rs7944435	0.89[ASN][1000 genomes]
rs7944578	0.85[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7949973	0.80[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9667574	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs972594	0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs9787851	0.83[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	nsv916534	chr11:9188436-9516241	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1055078	chr11:9252857-9538877	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
3	nsv427882	chr11:9431600-9626580	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
4	nsv1039537	chr11:9455387-9535970	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
5	nsv975149	chr11:9466591-9468624	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers	Chromatin interactive region miRNA target site	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8785	IPO7	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9419600-9471000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:9421000-9471200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:9423000-9470400	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:9424200-9470400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
5	chr11:9424800-9468600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
6	chr11:9424800-9469000	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:9424800-9470600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:9426200-9471600	Strong transcription	Dnd41	blood
9	chr11:9426800-9470600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr11:9427600-9471000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:9429800-9469000	Strong transcription	HUES6 Cell Line	embryonic stem cell
12	chr11:9430200-9470200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr11:9431800-9468800	Weak transcription	Stomach Mucosa	stomach
14	chr11:9434800-9470400	Strong transcription	Osteobl	bone
15	chr11:9435400-9470400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr11:9439600-9472000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:9439800-9470200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:9439800-9470600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr11:9440000-9470800	Strong transcription	Fetal Thymus	thymus
20	chr11:9440200-9470400	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr11:9443600-9470200	Strong transcription	HSMM	muscle
22	chr11:9443800-9470200	Strong transcription	HUVEC	blood vessel
23	chr11:9445400-9468600	Strong transcription	Fetal Intestine Large	intestine
24	chr11:9450600-9468600	Strong transcription	Liver	Liver
25	chr11:9452800-9480000	Weak transcription	Fetal Brain Male	brain
26	chr11:9453800-9470200	Strong transcription	Muscle Satellite Cultured Cells	--
27	chr11:9455200-9471600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:9456800-9471600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:9457800-9480600	Weak transcription	Psoas Muscle	Psoas
30	chr11:9459000-9468600	Strong transcription	A549	lung
31	chr11:9460800-9471000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr11:9460800-9472800	Weak transcription	Small Intestine	intestine
33	chr11:9461800-9474800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr11:9462200-9481000	Weak transcription	NHLF	lung
35	chr11:9463400-9471800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr11:9463400-9481000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr11:9463800-9470600	Weak transcription	Fetal Kidney	kidney
38	chr11:9463800-9473000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr11:9463800-9481000	Weak transcription	NHDF-Ad	bronchial
40	chr11:9464800-9480800	Weak transcription	HSMMtube	muscle
41	chr11:9465000-9468600	Weak transcription	Colonic Mucosa	Colon
42	chr11:9465000-9474400	Weak transcription	Colon Smooth Muscle	Colon
43	chr11:9465000-9480800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr11:9465000-9480800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr11:9465000-9481000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
46	chr11:9465200-9476000	Weak transcription	Aorta	Aorta
47	chr11:9465200-9481000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr11:9465200-9481200	Weak transcription	Ovary	ovary
49	chr11:9465400-9468800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr11:9465400-9469400	Weak transcription	NHEK	skin

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