Variant report

Variant	rs59785653
Chromosome Location	chr13:92414013-92414014
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs57666164	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58383288	0.84[AFR][1000 genomes]
rs58803517	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59669659	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59721804	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60085658	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73607624	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73607673	0.90[AFR][1000 genomes]
rs73609110	0.83[AFR][1000 genomes]
rs73609119	0.92[AFR][1000 genomes]
rs73609121	0.92[AFR][1000 genomes]
rs73609123	0.95[AFR][1000 genomes]
rs73609139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73609142	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73609143	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73609146	1.00[AMR][1000 genomes]
rs73609148	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73609164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73615684	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1042947	chr13:91571040-92416897	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
2	nsv541871	chr13:91571040-92416897	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1946 gene(s)	inside rSNPs	diseases
3	nsv1049382	chr13:92024240-92521180	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv541873	chr13:92024240-92521180	Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv2753383	chr13:92226599-92462699	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv529268	chr13:92267310-92531263	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv456065	chr13:92383193-92507887	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv562719	chr13:92383193-92507887	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv948820	chr13:92408505-92519053	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92383000-92419400	Weak transcription	Hela-S3	cervix
2	chr13:92413200-92414400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr13:92413600-92414200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:92414000-92414200	Enhancers	Fetal Intestine Large	intestine
5	chr13:92414000-92414400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:92414000-92417000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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