Variant report

Variant	rs9835551
Chromosome Location	chr3:161306754-161306755
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:13)

rs_ID	r²[population]
rs1399907	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73015256	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs73015264	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7623811	0.87[AFR][1000 genomes]
rs7625098	0.85[AMR][1000 genomes]
rs7649699	0.87[AFR][1000 genomes]
rs7652284	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9290086	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9826280	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9851467	0.87[AFR][1000 genomes]
rs9854161	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9863670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9873326	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
2	nsv829773	chr3:161150422-161315189	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv829774	chr3:161229405-161386919	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2422309	chr3:161242389-161425932	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv877711	chr3:161275848-161486665	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 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	chr3:161305000-161307400	Weak transcription	H9 Cell Line	embryonic stem cell

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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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