Variant report

Variant	rs34603830
Chromosome Location	chr13:69388003-69388004
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs9541590	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];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	nsv1049303	chr13:69238676-69923558	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1038918	chr13:69251052-69919763	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv541829	chr13:69251052-69919763	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2757540	chr13:69355636-69392579	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2759945	chr13:69355636-69392579	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv471145	chr13:69375632-69388776	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv3518742	chr13:69385694-69393561	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3518753	chr13:69385694-69393561	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv826691	chr13:69385796-69392970	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv818974	chr13:69387686-69391512	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69387000-69388200	Enhancers	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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