Variant report

Variant	rs9301896
Chromosome Location	chr13:94196062-94196063
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12184868	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1445267	0.94[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1584145	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1584146	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1584147	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs1900048	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1900049	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2166240	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2166241	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2166242	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2389006	1.00[ASN][1000 genomes]
rs2590509	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2590510	0.98[ASN][1000 genomes]
rs2590514	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2590515	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs2590517	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2813591	0.81[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2813593	0.98[ASN][1000 genomes]
rs2813597	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2892658	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3858838	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3858839	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4303337	0.98[ASN][1000 genomes]
rs4390456	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4439616	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4479094	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4491363	0.98[ASN][1000 genomes]
rs4548730	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4773749	0.94[EUR][1000 genomes]
rs6492665	0.93[ASN][1000 genomes]
rs7139968	0.98[ASN][1000 genomes]
rs7316980	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7322845	0.98[ASN][1000 genomes]
rs7332793	0.98[ASN][1000 genomes]
rs7337099	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7337720	0.90[ASN][1000 genomes]
rs7998884	0.93[ASN][1000 genomes]
rs8001786	0.98[ASN][1000 genomes]
rs9301886	0.97[ASN][1000 genomes]
rs9516247	0.84[AMR][1000 genomes];0.99[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	nsv869070	chr13:93347616-94286933	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1053035	chr13:93842576-94229732	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541880	chr13:93842576-94229732	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv530636	chr13:93997311-94281707	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv562749	chr13:94083352-94263206	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv948714	chr13:94100104-94699435	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv900922	chr13:94105666-94281492	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	esv2758340	chr13:94174654-94348179	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	esv2759958	chr13:94174654-94348179	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv933807	chr13:94187158-94845505	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94186800-94197000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:94192400-94203600	Weak transcription	Ovary	ovary
3	chr13:94192600-94212400	Weak transcription	HepG2	liver
4	chr13:94193200-94198800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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