Variant report

Variant	rs9920186
Chromosome Location	chr15:73383247-73383248
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1023924	0.83[CHD][hapmap]
rs1038137	0.83[JPT][hapmap]
rs10438294	0.87[GIH][hapmap]
rs10467948	0.83[JPT][hapmap]
rs10467949	0.93[CHB][hapmap];0.97[CHD][hapmap];0.96[GIH][hapmap];0.94[JPT][hapmap];0.94[ASN][1000 genomes]
rs1131854	0.89[CHB][hapmap];0.88[CHD][hapmap]
rs11632639	1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11636241	0.89[CHB][hapmap]
rs11639213	0.89[CHB][hapmap]
rs11856922	0.92[CEU][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12050774	0.80[CHD][hapmap]
rs12050848	0.94[CHB][hapmap];0.88[JPT][hapmap]
rs12708506	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs12899246	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs12902768	0.83[CHB][hapmap]
rs12907139	0.94[CHB][hapmap];0.93[JPT][hapmap]
rs12916928	0.98[ASN][1000 genomes]
rs13379875	0.80[CHD][hapmap]
rs1479337	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1479340	0.83[CHB][hapmap];0.97[CHD][hapmap]
rs1564345	0.83[CHB][hapmap];0.97[CHD][hapmap];0.83[JPT][hapmap]
rs17762600	0.83[CHD][hapmap]
rs17829830	0.83[CHD][hapmap]
rs1871385	0.83[CHB][hapmap];0.83[CHD][hapmap];0.84[GIH][hapmap]
rs2010793	0.94[ASN][1000 genomes]
rs2046017	0.94[CHB][hapmap];0.97[CHD][hapmap];0.83[JPT][hapmap]
rs2127277	0.83[CHB][hapmap];0.97[CHD][hapmap];0.83[JPT][hapmap]
rs2169951	0.83[JPT][hapmap]
rs2251205	0.94[CHB][hapmap];0.97[CHD][hapmap];0.89[JPT][hapmap]
rs2415147	0.83[CHB][hapmap]
rs28481558	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28743094	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28842482	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2899784	0.83[CHB][hapmap]
rs35060813	0.98[ASN][1000 genomes]
rs3736510	0.83[CHB][hapmap];0.82[CHD][hapmap];0.87[GIH][hapmap]
rs3743489	0.88[CHB][hapmap]
rs3784793	0.92[CHB][hapmap];0.88[JPT][hapmap]
rs4132535	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4132536	0.86[CHD][hapmap];0.83[JPT][hapmap]
rs4777582	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4777583	0.97[ASN][1000 genomes]
rs4777589	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];1.00[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4777590	0.83[CHD][hapmap];0.83[JPT][hapmap]
rs4777591	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58060856	0.81[ASN][1000 genomes]
rs6416501	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6416502	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6495047	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7164894	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7168555	0.83[CEU][hapmap];0.85[CHB][hapmap]
rs7169083	0.83[CHB][hapmap]
rs7172021	0.83[CHB][hapmap];0.97[CHD][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs7172396	0.82[CHB][hapmap];0.83[JPT][hapmap];0.81[ASN][1000 genomes]
rs7173142	1.00[ASN][1000 genomes]
rs7175329	1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs747872	0.83[CHB][hapmap]
rs747873	0.82[CHB][hapmap];0.83[CHD][hapmap];0.80[GIH][hapmap]
rs7495458	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8026121	0.83[JPT][hapmap]
rs8026579	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8027588	0.89[CHB][hapmap];0.91[CHD][hapmap]
rs8042700	0.83[CHB][hapmap]
rs922516	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];0.95[MEX][hapmap];0.99[MKK][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9672588	0.88[CHB][hapmap]

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	esv3352103	chr15:73191535-73454001	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv482421	chr15:73279141-73426897	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
3	nsv904338	chr15:73313691-73483718	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv517966	chr15:73349633-73488753	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv525462	chr15:73349633-73563495	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv904339	chr15:73375847-73483718	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv904340	chr15:73375847-73524629	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73371200-73388600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:73371200-73397000	Weak transcription	Pancreas	Pancrea
3	chr15:73371600-73393800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:73374200-73393600	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr15:73375600-73391200	Weak transcription	Brain Angular Gyrus	brain
6	chr15:73379600-73388600	Weak transcription	Fetal Intestine Small	intestine
7	chr15:73380200-73388800	Weak transcription	Fetal Intestine Large	intestine
8	chr15:73380400-73388600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr15:73383200-73383400	Enhancers	Psoas Muscle	Psoas

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