Variant report

Variant	rs72804801
Chromosome Location	chr5:152331031-152331032
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10515680	1.00[ASN][1000 genomes]
rs12153071	0.80[AMR][1000 genomes]
rs12153328	0.80[AMR][1000 genomes]
rs12186623	0.80[AMR][1000 genomes]
rs12188960	0.80[AMR][1000 genomes]
rs12516389	1.00[ASN][1000 genomes]
rs12517903	1.00[ASN][1000 genomes]
rs12518081	1.00[ASN][1000 genomes]
rs12654450	0.80[AMR][1000 genomes]
rs13154170	1.00[ASN][1000 genomes]
rs17488630	0.80[AMR][1000 genomes]
rs17489682	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17493121	1.00[ASN][1000 genomes]
rs17494099	1.00[ASN][1000 genomes]
rs34244108	1.00[ASN][1000 genomes]
rs34316705	1.00[ASN][1000 genomes]
rs35029802	1.00[ASN][1000 genomes]
rs35708928	1.00[ASN][1000 genomes]
rs4394168	0.81[AMR][1000 genomes]
rs4437425	0.80[AMR][1000 genomes]
rs55992747	0.80[AMR][1000 genomes]
rs56117655	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6863497	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs71588075	1.00[ASN][1000 genomes]
rs71588077	1.00[ASN][1000 genomes]
rs72802852	0.80[AMR][1000 genomes]
rs72802853	0.80[AMR][1000 genomes]
rs72802868	0.80[AMR][1000 genomes]
rs72802874	0.80[AMR][1000 genomes]
rs72802883	0.80[AMR][1000 genomes]
rs72804778	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72804786	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs72804798	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72804800	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72806703	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72806705	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7443245	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023676	chr5:151979253-152925064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv537927	chr5:151979253-152925064	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv883049	chr5:152159184-152399894	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv600089	chr5:152200109-152488891	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1017812	chr5:152220845-152467431	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv537928	chr5:152220845-152467431	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1017488	chr5:152239716-152383640	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv883050	chr5:152277537-152540026	Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv516577	chr5:152324701-152360494	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv883051	chr5:152327668-152409232	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152330800-152331200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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