Variant report

Variant	rs568430
Chromosome Location	chr1:72083896-72083897
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10749801	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs10749802	0.97[AFR][1000 genomes]
rs10789320	1.00[ASW][hapmap];0.85[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap]
rs10889925	1.00[ASW][hapmap];0.85[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs10889926	0.89[YRI][hapmap]
rs11209819	1.00[ASW][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs12086374	0.89[YRI][hapmap]
rs1213512	1.00[YRI][hapmap]
rs1237570	0.97[AFR][1000 genomes]
rs1334986	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs13375194	0.90[YRI][hapmap]
rs13376015	0.89[YRI][hapmap]
rs1413951	1.00[YRI][hapmap]
rs1414070	1.00[YRI][hapmap]
rs1628661	1.00[YRI][hapmap]
rs1674954	0.97[AFR][1000 genomes]
rs1760607	1.00[AFR][1000 genomes]
rs1762723	0.92[AFR][1000 genomes]
rs1762733	0.97[AFR][1000 genomes]
rs1762735	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs1932176	1.00[YRI][hapmap]
rs2152218	1.00[YRI][hapmap]
rs2422018	0.97[AFR][1000 genomes]
rs2483663	0.97[AFR][1000 genomes]
rs2483664	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2611625	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2637688	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2637689	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2781151	0.97[AFR][1000 genomes]
rs2783044	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2783045	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2783050	1.00[ASW][hapmap];1.00[LWK][hapmap];0.88[AFR][1000 genomes]
rs2794308	1.00[ASW][hapmap];0.85[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs2991329	0.86[ASW][hapmap];1.00[LWK][hapmap];0.88[AFR][1000 genomes]
rs2992131	0.97[AFR][1000 genomes]
rs4556309	0.97[AFR][1000 genomes]
rs484724	0.82[YRI][hapmap]
rs492016	1.00[ASW][hapmap];0.85[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs500847	0.88[AFR][1000 genomes]
rs503093	0.88[AFR][1000 genomes]
rs523835	0.88[AFR][1000 genomes]
rs553162	0.97[AFR][1000 genomes]
rs564363	1.00[ASW][hapmap];1.00[LWK][hapmap];0.83[MKK][hapmap];0.85[AFR][1000 genomes]
rs637576	1.00[ASW][hapmap];0.85[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap]
rs6661576	1.00[YRI][hapmap]
rs6663352	1.00[YRI][hapmap];0.97[AFR][1000 genomes]
rs6679523	0.89[YRI][hapmap]
rs693808	1.00[ASW][hapmap];0.85[LWK][hapmap];1.00[MKK][hapmap];0.90[YRI][hapmap];0.92[AFR][1000 genomes]
rs7513706	0.97[AFR][1000 genomes]
rs7553341	0.89[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949599	chr1:71655652-72327802	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1007250	chr1:71998391-72350683	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv534992	chr1:71998391-72350683	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv948821	chr1:72049987-72477221	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1003446	chr1:72060680-72419918	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv461884	chr1:72077549-72238691	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv546476	chr1:72077549-72238691	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv461895	chr1:72079898-72206799	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv546477	chr1:72079898-72206799	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv1006188	chr1:72081620-72215373	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv534993	chr1:72081620-72215373	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72072200-72085200	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:72081000-72087000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr1:72083400-72084000	Enhancers	Fetal Stomach	stomach
4	chr1:72083600-72084000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:72083600-72084200	Enhancers	Pancreas	Pancrea

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