Variant report

Variant	rs9302151
Chromosome Location	chr15:50290361-50290362
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:50277715..50280459-chr15:50288291..50290867,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11070741	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12591825	0.92[GIH][hapmap];0.81[TSI][hapmap]
rs12593937	0.82[GIH][hapmap]
rs2413992	0.82[GIH][hapmap]
rs2413997	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2414001	0.89[GIH][hapmap];0.81[TSI][hapmap]
rs2414002	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2414004	1.00[CEU][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2414005	1.00[ASW][hapmap];1.00[CEU][hapmap];0.81[MEX][hapmap];0.91[MKK][hapmap];0.91[TSI][hapmap];0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2414006	1.00[ASW][hapmap];1.00[CEU][hapmap];0.97[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2414008	1.00[CEU][hapmap];0.94[GIH][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4343223	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4520793	1.00[LWK][hapmap]
rs4550392	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4583186	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4627270	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs57498160	0.85[AMR][1000 genomes]
rs6493393	0.82[ASW][hapmap];0.85[GIH][hapmap];0.91[MEX][hapmap];0.97[MKK][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6493394	0.96[CEU][hapmap];1.00[GIH][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7165307	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7176999	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7177104	0.89[GIH][hapmap];0.83[MEX][hapmap];0.83[TSI][hapmap]
rs7179614	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7182041	0.92[GIH][hapmap];0.83[MEX][hapmap];0.81[TSI][hapmap]
rs8027073	0.82[GIH][hapmap]
rs8028408	0.83[EUR][1000 genomes]
rs8041014	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][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	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1035983	chr15:50223334-50595170	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv542382	chr15:50223334-50595170	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv904207	chr15:50290295-50352945	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9302151	MFAP1	cis	cerebellum	SCAN

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50268600-50290400	Strong transcription	Primary hematopoietic stem cells	blood
2	chr15:50278000-50301600	Weak transcription	Liver	Liver
3	chr15:50282000-50295600	Weak transcription	Adipose Nuclei	Adipose
4	chr15:50282200-50290400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
5	chr15:50283000-50290800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr15:50283400-50290400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr15:50287400-50294400	Weak transcription	Fetal Stomach	stomach
8	chr15:50287600-50296000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr15:50288400-50294000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr15:50288600-50293600	Weak transcription	Colon Smooth Muscle	Colon
11	chr15:50289600-50291800	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr15:50290000-50291800	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr15:50290200-50291600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr15:50290200-50291800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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