Variant report

Variant	rs11957616
Chromosome Location	chr5:42530196-42530197
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:42524054..42526820-chr5:42527657..42530320,2	K562	blood:
2	chr5:42522021..42523658-chr5:42528287..42530323,2	MCF-7	breast:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10755268	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1117110	0.91[EUR][1000 genomes]
rs11738365	0.81[CEU][hapmap];0.90[EUR][1000 genomes]
rs11742495	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11747975	0.80[CEU][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11748366	1.00[CEU][hapmap];0.81[LWK][hapmap];0.81[MKK][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13162973	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1396768	0.87[EUR][1000 genomes]
rs1396773	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1467049	0.81[CEU][hapmap];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1509452	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1509453	0.80[MKK][hapmap];1.00[ASN][1000 genomes]
rs1509455	0.87[EUR][1000 genomes]
rs1509456	0.87[EUR][1000 genomes]
rs1567374	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1605848	0.81[EUR][1000 genomes]
rs1605851	0.91[EUR][1000 genomes]
rs1858136	0.87[EUR][1000 genomes]
rs1858137	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1858139	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1876788	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1876790	0.87[EUR][1000 genomes]
rs1912107	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1960498	0.81[CEU][hapmap];0.91[EUR][1000 genomes]
rs2036745	0.81[CEU][hapmap];0.93[EUR][1000 genomes]
rs2175126	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2202883	0.90[EUR][1000 genomes]
rs2221712	0.90[EUR][1000 genomes]
rs2395970	0.91[EUR][1000 genomes]
rs2940912	0.87[EUR][1000 genomes]
rs2940914	0.91[EUR][1000 genomes]
rs2940916	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2940917	0.81[CEU][hapmap];0.93[EUR][1000 genomes]
rs2940918	0.81[CEU][hapmap];0.93[EUR][1000 genomes]
rs2940919	0.81[CEU][hapmap];0.88[EUR][1000 genomes]
rs2940920	0.81[CEU][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2940922	0.81[CEU][hapmap];0.93[EUR][1000 genomes]
rs2940926	0.81[CEU][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2940929	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2940931	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2940934	0.91[EUR][1000 genomes]
rs2940935	0.91[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2940939	0.86[EUR][1000 genomes]
rs2940942	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2940943	0.91[CEU][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972391	1.00[ASN][1000 genomes]
rs2972395	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972400	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972404	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972406	0.88[EUR][1000 genomes]
rs2972407	0.81[CEU][hapmap];0.91[EUR][1000 genomes]
rs2972410	0.93[EUR][1000 genomes]
rs2972411	0.81[CEU][hapmap];0.93[EUR][1000 genomes]
rs2972412	0.80[CEU][hapmap];0.93[EUR][1000 genomes]
rs2972413	0.81[CEU][hapmap];0.93[EUR][1000 genomes]
rs2972414	0.87[EUR][1000 genomes]
rs2972415	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972416	0.81[CEU][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2972417	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972419	0.91[CEU][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34509769	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4642376	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4866890	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58416991	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58960035	1.00[ASN][1000 genomes]
rs60126365	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61636452	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62370642	1.00[ASN][1000 genomes]
rs62370646	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62370648	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6451614	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6876736	1.00[CEU][hapmap];0.81[LWK][hapmap];0.82[MKK][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6881436	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6884737	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7379192	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7704355	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7728337	0.81[CEU][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9686286	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs974051	0.91[CEU][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[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	nsv933208	chr5:41879946-42876624	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
2	nsv492147	chr5:41902086-42896162	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
3	nsv1020464	chr5:42488628-42699394	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1018751	chr5:42491883-42697923	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42522400-42532000	Weak transcription	Liver	Liver
2	chr5:42525000-42531800	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr5:42525400-42531800	Weak transcription	Psoas Muscle	Psoas
4	chr5:42529800-42531400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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