Variant report

Variant	rs12587051
Chromosome Location	chr14:66844437-66844438
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:66588446..66589156-chr14:66844160..66844957,2	MCF-7	breast:
2	chr14:66826252..66826789-chr14:66844012..66844547,2	MCF-7	breast:

Extended variants
information (count: 148 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:138)

rs_ID	r²[population]
rs1010965	0.81[ASN][1000 genomes]
rs10129809	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs10133769	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs10134043	0.91[CHB][hapmap]
rs10134278	0.91[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs10135880	0.84[ASN][1000 genomes]
rs10142124	0.82[ASN][1000 genomes]
rs10142143	0.81[ASN][1000 genomes]
rs10142195	0.81[ASN][1000 genomes]
rs10142375	0.82[ASN][1000 genomes]
rs10143291	0.87[CHB][hapmap]
rs10144449	0.91[CHB][hapmap]
rs10146361	0.84[ASN][1000 genomes]
rs10148021	0.84[ASN][1000 genomes]
rs10148290	0.91[CHB][hapmap]
rs10148418	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs10149072	0.84[ASN][1000 genomes]
rs10151844	0.80[ASN][1000 genomes]
rs10152053	0.80[ASN][1000 genomes]
rs10220636	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs12050456	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12586868	1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[ASN][1000 genomes]
rs12588173	0.80[ASN][1000 genomes]
rs12588449	0.83[ASN][1000 genomes]
rs12588933	0.80[ASN][1000 genomes]
rs12589479	0.80[ASN][1000 genomes]
rs12590545	0.80[ASN][1000 genomes]
rs13353130	0.80[ASN][1000 genomes]
rs13379248	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1379413	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs1379414	0.81[ASN][1000 genomes]
rs1379416	0.80[ASN][1000 genomes]
rs1457419	0.91[CHB][hapmap]
rs1457420	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs1457422	0.91[CHB][hapmap]
rs1457423	0.91[CHB][hapmap];0.83[JPT][hapmap]
rs1457424	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs1457425	0.82[ASN][1000 genomes]
rs1457426	0.82[ASN][1000 genomes]
rs1457427	0.82[ASN][1000 genomes]
rs1457428	0.84[ASN][1000 genomes]
rs1457429	0.84[ASN][1000 genomes]
rs1457430	0.84[ASN][1000 genomes]
rs1457431	0.81[ASN][1000 genomes]
rs1457432	0.80[ASN][1000 genomes]
rs1457433	0.80[ASN][1000 genomes]
rs1457434	0.82[ASN][1000 genomes]
rs1457437	0.80[ASN][1000 genomes]
rs1457439	0.84[ASN][1000 genomes]
rs1598772	0.82[ASN][1000 genomes]
rs17103525	0.80[ASN][1000 genomes]
rs17827222	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17827252	0.88[ASN][1000 genomes]
rs17827349	0.80[ASN][1000 genomes]
rs17827523	0.80[ASN][1000 genomes]
rs17827735	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs17827741	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs17827790	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs1902644	0.80[ASN][1000 genomes]
rs1959672	0.84[ASN][1000 genomes]
rs2085482	0.81[ASN][1000 genomes]
rs2297620	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs2319184	0.92[ASN][1000 genomes]
rs2319185	0.82[ASN][1000 genomes]
rs2319387	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs28408630	0.84[ASN][1000 genomes]
rs28772914	0.80[ASN][1000 genomes]
rs28802324	0.80[ASN][1000 genomes]
rs3737160	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs3737161	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs3742853	0.84[ASN][1000 genomes]
rs3818770	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs4600407	0.84[ASN][1000 genomes]
rs6573666	0.84[ASN][1000 genomes]
rs6573667	0.85[ASN][1000 genomes]
rs6573668	0.84[ASN][1000 genomes]
rs6573669	0.84[ASN][1000 genomes]
rs6573670	0.85[ASN][1000 genomes]
rs6573671	0.80[ASN][1000 genomes]
rs6573679	0.86[CHB][hapmap]
rs7140509	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7141089	0.81[ASN][1000 genomes]
rs7142097	0.91[CHB][hapmap]
rs7143629	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs7143823	0.91[CHB][hapmap]
rs7145556	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs7146723	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7147360	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7148998	0.87[YRI][hapmap]
rs7149352	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7149488	0.84[ASN][1000 genomes]
rs7149651	0.80[ASN][1000 genomes]
rs7149668	0.91[CHB][hapmap]
rs7150098	0.80[ASN][1000 genomes]
rs7150418	0.81[ASN][1000 genomes]
rs7150773	0.86[ASN][1000 genomes]
rs7151102	0.91[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs7151773	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs7154154	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs7155944	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7156737	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7157060	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7158262	0.80[ASN][1000 genomes]
rs7159364	0.80[ASN][1000 genomes]
rs7159681	0.80[ASN][1000 genomes]
rs7159750	0.80[ASN][1000 genomes]
rs7159796	0.91[CHB][hapmap];0.81[JPT][hapmap]
rs7160107	0.84[ASN][1000 genomes]
rs7160183	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7160519	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs7160696	0.80[ASN][1000 genomes]
rs716232	0.80[ASN][1000 genomes]
rs716233	0.80[ASN][1000 genomes]
rs716234	0.80[ASN][1000 genomes]
rs73273971	0.84[ASN][1000 genomes]
rs7359115	0.84[ASN][1000 genomes]
rs735957	0.80[ASN][1000 genomes]
rs8004227	0.80[ASN][1000 genomes]
rs8004856	0.85[ASN][1000 genomes]
rs8005737	0.85[ASN][1000 genomes]
rs8007262	0.81[ASN][1000 genomes]
rs8007305	0.84[ASN][1000 genomes]
rs8009108	0.84[ASN][1000 genomes]
rs8009415	0.83[ASN][1000 genomes]
rs8012649	0.85[ASN][1000 genomes]
rs8013806	0.83[ASN][1000 genomes]
rs8015155	0.80[ASN][1000 genomes]
rs8018685	0.84[ASN][1000 genomes]
rs8020024	0.82[ASN][1000 genomes]
rs8020115	0.81[ASN][1000 genomes]
rs8020532	0.80[ASN][1000 genomes]
rs8021204	0.84[ASN][1000 genomes]
rs8181963	0.84[ASN][1000 genomes]
rs8181967	0.84[ASN][1000 genomes]
rs928553	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9323473	0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9635252	0.80[ASN][1000 genomes]
rs9635253	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv564953	chr14:66287921-67046960	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv1050485	chr14:66308283-67109270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
4	nsv530775	chr14:66316836-67079049	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
5	nsv530793	chr14:66317036-67078908	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv1046455	chr14:66345369-66848234	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
7	nsv1043864	chr14:66372458-66845503	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
8	esv3385263	chr14:66514718-67511481	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
9	nsv983837	chr14:66619600-67014519	Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	nsv933275	chr14:66649843-67024881	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66826600-66846200	Weak transcription	Fetal Brain Male	brain
2	chr14:66836600-66845000	Weak transcription	Pancreas	Pancrea
3	chr14:66840600-66851000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr14:66841400-66845600	Weak transcription	GM12878-XiMat	blood
5	chr14:66842200-66848600	Weak transcription	Fetal Brain Female	brain
6	chr14:66842400-66850800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr14:66843000-66845400	Weak transcription	Brain Germinal Matrix	brain
8	chr14:66843600-66846600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:66844200-66845400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr14:66844200-66845400	Weak transcription	Liver	Liver

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