Variant report

Variant	rs17621796
Chromosome Location	chr4:20642151-20642152
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10017693	1.00[CHB][hapmap]
rs10022322	1.00[CHB][hapmap]
rs10024002	1.00[CHB][hapmap]
rs10938801	1.00[CHB][hapmap];0.82[ASN][1000 genomes]
rs10938804	0.81[JPT][hapmap]
rs11932551	0.83[ASN][1000 genomes]
rs12640448	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs12641186	0.94[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs12645674	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16869851	0.82[ASN][1000 genomes]
rs17551335	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17622163	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17622371	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2052775	1.00[CHB][hapmap]
rs2162413	0.85[CEU][hapmap]
rs2288308	1.00[CHB][hapmap]
rs28374411	0.89[ASN][1000 genomes]
rs3764967	1.00[CEU][hapmap];0.88[CHB][hapmap]
rs55794413	0.82[ASN][1000 genomes]
rs55874299	0.82[ASN][1000 genomes]
rs56152829	0.82[ASN][1000 genomes]
rs56237079	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61790748	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62410065	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62410092	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62410099	0.82[ASN][1000 genomes]
rs6811505	0.88[CHB][hapmap]
rs6824850	0.87[ASN][1000 genomes]
rs6831516	0.85[CHB][hapmap]
rs725594	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs755155	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7655154	1.00[CHB][hapmap]
rs7681691	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs9995697	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829875	chr4:20502895-20680956	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	89 gene(s)	inside rSNPs	diseases
2	nsv1013077	chr4:20599841-20732558	Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1010145	chr4:20601908-21057992	ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv537052	chr4:20601908-21057992	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
5	nsv1014941	chr4:20611726-21345226	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv537053	chr4:20611726-21345226	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv829876	chr4:20638736-20835621	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 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	chr4:20641800-20642200	Enhancers	Sigmoid Colon	Sigmoid Colon
2	chr4:20642000-20647400	Weak transcription	Liver	Liver

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