Variant report

Variant	rs2006635
Chromosome Location	chr7:78623138-78623139
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1006818	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10215372	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10224582	0.89[CHB][hapmap]
rs10224972	0.89[CEU][hapmap]
rs10226001	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10236354	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10259881	0.89[CEU][hapmap]
rs10269689	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs10808175	0.95[EUR][1000 genomes]
rs11769552	0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs12113491	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12534480	0.89[CEU][hapmap];0.88[EUR][1000 genomes]
rs12536821	0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12536843	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12538053	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12539532	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs12540352	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12540925	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12669763	0.95[EUR][1000 genomes]
rs12705911	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13438061	0.85[CEU][hapmap]
rs1476106	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2078428	0.81[CEU][hapmap]
rs2079955	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2098180	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2098181	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2109713	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2159687	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2191724	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs2191726	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2191727	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2191728	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2191730	0.82[CHB][hapmap]
rs2215546	0.89[CEU][hapmap]
rs2215547	0.90[CEU][hapmap]
rs2280607	0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2280608	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2363930	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2363931	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs28572181	0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs28716458	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs34086589	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4727794	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs4727796	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4730596	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs4730597	0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4730599	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4730601	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4730619	0.94[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs5004248	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6466468	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs6466471	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6466477	0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6945664	1.00[JPT][hapmap]
rs6952133	0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6964007	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs727652	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7779315	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7781812	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7789063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7791770	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7792974	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7793390	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs7795421	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7797398	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7799032	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7805367	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7807319	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7809089	0.89[CEU][hapmap];0.90[EUR][1000 genomes]
rs9656215	0.89[EUR][1000 genomes]
rs984312	0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[ASN][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	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv482826	chr7:78548319-78717605	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv471642	chr7:78548320-78717605	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1029799	chr7:78608097-79061737	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78614000-78632400	Weak transcription	Aorta	Aorta
2	chr7:78622800-78623400	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr7:78622800-78623600	Enhancers	Brain Anterior Caudate	brain
4	chr7:78622800-78623600	Enhancers	Fetal Kidney	kidney
5	chr7:78622800-78624000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:78622800-78624000	Enhancers	Brain Substantia Nigra	brain
7	chr7:78623000-78624000	Enhancers	Brain Hippocampus Middle	brain

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