Variant report

Variant	rs10939887
Chromosome Location	chr5:60531720-60531721
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs4428365	1.00[EUR][1000 genomes]
rs4458537	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4505907	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs61288496	0.91[EUR][1000 genomes]
rs61554378	0.83[EUR][1000 genomes]
rs6866414	0.83[EUR][1000 genomes]
rs6892223	0.91[EUR][1000 genomes]
rs7446462	0.91[EUR][1000 genomes]
rs764066	0.91[EUR][1000 genomes]
rs764067	0.91[EUR][1000 genomes]
rs9291708	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9291709	1.00[EUR][1000 genomes]
rs9291711	1.00[EUR][1000 genomes]
rs9885353	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	nsv1034038	chr5:60375328-60607654	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv1028884	chr5:60414723-60732779	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	46 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	chr5:60529600-60533000	Weak transcription	Fetal Brain Male	brain

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

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