Variant report

Variant	rs648360
Chromosome Location	chr6:101362843-101362844
allele	C/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:67)

rs_ID	r²[population]
rs10485297	0.90[ASN][1000 genomes]
rs11155726	0.84[EUR][1000 genomes]
rs12189857	0.82[EUR][1000 genomes]
rs17054315	0.90[ASN][1000 genomes]
rs17061158	0.84[ASN][1000 genomes]
rs17061168	0.85[ASN][1000 genomes]
rs17061190	0.90[ASN][1000 genomes]
rs17061191	0.90[ASN][1000 genomes]
rs17061195	0.90[ASN][1000 genomes]
rs17061206	0.90[ASN][1000 genomes]
rs17061209	0.83[EUR][1000 genomes]
rs17061230	1.00[EUR][1000 genomes]
rs17061234	0.99[ASN][1000 genomes]
rs17061235	0.99[ASN][1000 genomes]
rs17061236	0.99[ASN][1000 genomes]
rs17061242	0.99[ASN][1000 genomes]
rs17061360	0.89[ASN][1000 genomes]
rs17061363	0.89[ASN][1000 genomes]
rs17061371	0.88[ASN][1000 genomes]
rs17061406	0.83[ASN][1000 genomes]
rs17673031	0.82[EUR][1000 genomes]
rs2180339	0.96[ASN][1000 genomes]
rs2756040	1.00[EUR][1000 genomes]
rs4427005	0.99[ASN][1000 genomes]
rs4637650	0.84[ASN][1000 genomes]
rs592463	1.00[EUR][1000 genomes]
rs600653	0.98[EUR][1000 genomes]
rs601360	0.87[EUR][1000 genomes]
rs606032	1.00[EUR][1000 genomes]
rs609522	1.00[EUR][1000 genomes]
rs612459	0.87[EUR][1000 genomes]
rs613338	0.87[EUR][1000 genomes]
rs614094	1.00[ASN][1000 genomes]
rs617365	1.00[EUR][1000 genomes]
rs625745	1.00[EUR][1000 genomes]
rs626411	0.93[EUR][1000 genomes]
rs635258	1.00[EUR][1000 genomes]
rs640315	1.00[EUR][1000 genomes]
rs668932	0.98[EUR][1000 genomes]
rs673119	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs673138	0.96[EUR][1000 genomes]
rs674589	0.98[EUR][1000 genomes]
rs67917362	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs705598	0.82[EUR][1000 genomes]
rs705601	0.83[EUR][1000 genomes]
rs705602	0.84[EUR][1000 genomes]
rs705609	0.83[EUR][1000 genomes]
rs705612	1.00[EUR][1000 genomes]
rs705618	1.00[EUR][1000 genomes]
rs705619	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs705620	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72942892	0.91[EUR][1000 genomes]
rs72946427	1.00[EUR][1000 genomes]
rs72947091	0.82[EUR][1000 genomes]
rs72951137	0.84[EUR][1000 genomes]
rs72951161	0.87[EUR][1000 genomes]
rs73508859	0.99[ASN][1000 genomes]
rs73760737	0.99[ASN][1000 genomes]
rs73760738	0.99[ASN][1000 genomes]
rs768985	0.99[ASN][1000 genomes]
rs7755696	1.00[EUR][1000 genomes]
rs846784	0.82[EUR][1000 genomes]
rs846790	1.00[EUR][1000 genomes]
rs846796	1.00[EUR][1000 genomes]
rs861752	0.82[EUR][1000 genomes]
rs9485429	0.99[ASN][1000 genomes]
rs9498435	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1020692	chr6:101136992-101426071	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv886457	chr6:101158950-101487473	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv1019213	chr6:101225650-101623140	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
7	nsv538391	chr6:101225650-101623140	Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
8	esv2763587	chr6:101277874-101510491	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv981366	chr6:101350432-101366644	Active TSS Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101362000-101367600	Weak transcription	Fetal Intestine Small	intestine
2	chr6:101362400-101363800	Weak transcription	K562	blood

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