Variant report

Variant	rs7132930
Chromosome Location	chr12:9137288-9137289
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10129061	0.91[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10400563	0.87[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10743568	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10771238	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10842660	0.83[CHB][hapmap]
rs11048195	0.91[CHB][hapmap]
rs11048337	0.87[CHB][hapmap]
rs11048338	0.91[CHB][hapmap];0.82[CHD][hapmap]
rs11048414	0.89[ASN][1000 genomes]
rs1121401	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11614202	0.82[EUR][1000 genomes]
rs12821842	0.91[CHB][hapmap];0.82[CHD][hapmap]
rs12823100	0.91[CHB][hapmap]
rs1476911	0.86[CHB][hapmap]
rs1805248	0.95[CHB][hapmap]
rs1805721	0.83[CHB][hapmap];0.82[CHD][hapmap]
rs1805722	0.83[CHB][hapmap]
rs1805723	0.83[CHB][hapmap];0.82[CHD][hapmap]
rs1805724	0.91[CHB][hapmap]
rs1805725	1.00[ASW][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.82[TSI][hapmap];0.95[YRI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1805727	0.92[ASW][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.84[MKK][hapmap];0.82[TSI][hapmap];0.95[YRI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1805732	0.86[CHB][hapmap]
rs1805733	0.86[CHB][hapmap]
rs1805735	0.91[CHB][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs1805754	0.95[CHB][hapmap];0.95[CHD][hapmap];0.90[JPT][hapmap];0.83[ASN][1000 genomes]
rs1805761	0.91[CHB][hapmap]
rs2080116	0.83[CHB][hapmap]
rs2284349	0.85[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2377671	0.83[ASN][1000 genomes]
rs2377676	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4309200	0.91[CHB][hapmap];0.82[CHD][hapmap]
rs4639983	0.91[CEU][hapmap];0.95[CHB][hapmap];0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4883203	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6832	0.91[CHB][hapmap]
rs7961355	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7974486	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs933462	0.91[CHB][hapmap]
rs987917	0.95[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832327	chr12:9081779-9246220	Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription 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	25 gene(s)	inside rSNPs	diseases
2	nsv1045317	chr12:9113216-9544655	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	38 gene(s)	inside rSNPs	diseases
3	nsv819596	chr12:9113514-9141537	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv2754892	chr12:9136351-9179007	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs7132930	M6PR	cis	lung	GTEx
rs7132930	CD163	cis	parietal	SCAN
rs7132930	C12orf59	cis	parietal	SCAN

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9133200-9139800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr12:9133600-9138200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:9133600-9140600	Weak transcription	Spleen	Spleen
4	chr12:9133800-9139000	Weak transcription	Primary T cells from cord blood	blood
5	chr12:9133800-9164600	Weak transcription	Psoas Muscle	Psoas
6	chr12:9133800-9170200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr12:9135000-9138400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:9135800-9141800	Weak transcription	Primary B cells from cord blood	blood
9	chr12:9136400-9137600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
10	chr12:9136800-9137400	Enhancers	Primary T cells fromperipheralblood	blood
11	chr12:9136800-9137400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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