Variant report

Variant	rs10105606
Chromosome Location	chr8:19827848-19827849
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 114 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:109)

rs_ID	r²[population]
rs11986942	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13702	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.88[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1372340	0.90[ASN][1000 genomes]
rs1372341	0.82[ASN][1000 genomes]
rs1372343	0.90[ASN][1000 genomes]
rs1372344	0.99[ASN][1000 genomes]
rs1441753	0.99[ASN][1000 genomes]
rs1441754	0.98[ASN][1000 genomes]
rs1441755	0.99[ASN][1000 genomes]
rs1441756	0.99[ASN][1000 genomes]
rs1441757	0.99[ASN][1000 genomes]
rs1441758	0.99[ASN][1000 genomes]
rs1441762	0.99[ASN][1000 genomes]
rs1441763	0.99[ASN][1000 genomes]
rs1441764	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1441766	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs15285	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.91[TSI][hapmap]
rs1569213	0.88[ASN][1000 genomes]
rs17411031	0.99[ASN][1000 genomes]
rs17411045	0.99[ASN][1000 genomes]
rs17411126	0.99[ASN][1000 genomes]
rs17411133	0.99[ASN][1000 genomes]
rs17411168	0.99[ASN][1000 genomes]
rs17489268	0.99[ASN][1000 genomes]
rs17489282	0.99[ASN][1000 genomes]
rs17489373	0.99[ASN][1000 genomes]
rs17489539	0.89[ASN][1000 genomes]
rs1819092	0.86[ASN][1000 genomes]
rs1819094	0.82[ASN][1000 genomes]
rs1822200	0.99[ASN][1000 genomes]
rs1837842	0.99[ASN][1000 genomes]
rs1837843	0.99[ASN][1000 genomes]
rs1919484	0.98[ASN][1000 genomes]
rs1992442	0.99[ASN][1000 genomes]
rs1992443	0.99[ASN][1000 genomes]
rs2009493	0.99[ASN][1000 genomes]
rs2083636	0.99[ASN][1000 genomes]
rs2083637	0.99[ASN][1000 genomes]
rs2119689	0.99[ASN][1000 genomes]
rs2165558	0.91[ASN][1000 genomes]
rs2410618	0.99[ASN][1000 genomes]
rs2410619	0.99[ASN][1000 genomes]
rs2410620	0.97[ASN][1000 genomes]
rs2410621	0.97[ASN][1000 genomes]
rs2410623	0.99[ASN][1000 genomes]
rs2410625	0.99[ASN][1000 genomes]
rs2410627	0.91[ASN][1000 genomes]
rs2410628	0.89[ASN][1000 genomes]
rs2410629	0.91[ASN][1000 genomes]
rs2410630	0.88[ASN][1000 genomes]
rs287	0.93[ASN][1000 genomes]
rs289	0.93[ASN][1000 genomes]
rs2898495	0.91[ASN][1000 genomes]
rs291	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs295	0.93[ASN][1000 genomes]
rs297	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs301	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs304	0.95[ASN][1000 genomes]
rs305	0.95[ASN][1000 genomes]
rs314	0.81[AFR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs320	0.95[ASN][1000 genomes]
rs3208305	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs322	0.95[ASN][1000 genomes]
rs326	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.85[TSI][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs327	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs331	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs34327087	0.99[ASN][1000 genomes]
rs34345068	0.99[ASN][1000 genomes]
rs34499461	0.98[ASN][1000 genomes]
rs34564316	0.99[ASN][1000 genomes]
rs34693282	0.90[ASN][1000 genomes]
rs34932218	0.99[ASN][1000 genomes]
rs34942551	0.98[ASN][1000 genomes]
rs35237252	0.96[ASN][1000 genomes]
rs35369244	0.98[ASN][1000 genomes]
rs35465966	0.90[ASN][1000 genomes]
rs35495249	0.99[ASN][1000 genomes]
rs35617716	0.96[ASN][1000 genomes]
rs35687633	0.99[ASN][1000 genomes]
rs35739466	0.98[ASN][1000 genomes]
rs3844510	0.99[ASN][1000 genomes]
rs3916027	1.00[ASN][1000 genomes]
rs4083261	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4126104	0.99[ASN][1000 genomes]
rs4320561	0.97[ASN][1000 genomes]
rs4333617	0.88[ASN][1000 genomes]
rs4335137	0.86[ASN][1000 genomes]
rs4375019	0.88[ASN][1000 genomes]
rs4406409	0.99[ASN][1000 genomes]
rs4425772	0.99[ASN][1000 genomes]
rs4593558	0.91[ASN][1000 genomes]
rs4628269	0.99[ASN][1000 genomes]
rs4644277	0.99[ASN][1000 genomes]
rs4922117	0.99[ASN][1000 genomes]
rs4922118	0.89[ASN][1000 genomes]
rs4922119	0.89[ASN][1000 genomes]
rs6586886	0.88[ASN][1000 genomes]
rs6986010	0.89[ASN][1000 genomes]
rs7013777	0.86[ASN][1000 genomes]
rs73208815	0.88[ASN][1000 genomes]
rs7461115	0.91[ASN][1000 genomes]
rs765547	0.99[ASN][1000 genomes]
rs765548	0.99[ASN][1000 genomes]
rs765549	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs894211	0.99[ASN][1000 genomes]
rs920588	0.99[ASN][1000 genomes]
rs920589	0.99[ASN][1000 genomes]
rs9644637	0.99[ASN][1000 genomes]
rs9644638	0.99[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	nsv610759	chr8:19561997-20068842	Enhancers Strong transcription Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv498082	chr8:19722435-19873112	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
3	esv32767	chr8:19740189-19873082	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv890632	chr8:19816371-19853146	Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Triglycerides	20864672	GWAS catalog

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19820600-19833400	Weak transcription	Psoas Muscle	Psoas
2	chr8:19823400-19828200	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:19824800-19830000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr8:19826200-19828800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr8:19826600-19828400	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr8:19827800-19828000	Enhancers	Adipose Nuclei	Adipose

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