Variant report

Variant	rs6885474
Chromosome Location	chr5:113443016-113443017
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs17136194	1.00[EUR][1000 genomes]
rs17136271	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17136278	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2974457	1.00[EUR][1000 genomes]
rs56823850	1.00[EUR][1000 genomes]
rs57178641	1.00[EUR][1000 genomes]
rs61188125	1.00[EUR][1000 genomes]
rs6867558	1.00[EUR][1000 genomes]
rs6876006	1.00[EUR][1000 genomes]
rs6881490	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73256306	1.00[EUR][1000 genomes]
rs73256373	1.00[EUR][1000 genomes]
rs73779586	1.00[EUR][1000 genomes]
rs73779601	1.00[EUR][1000 genomes]
rs73782123	1.00[EUR][1000 genomes]
rs7716446	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882726	chr5:113404933-113555626	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1020064	chr5:113418512-113492951	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	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	chr5:113443000-113446200	Weak transcription	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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