Variant report

Variant	rs57279729
Chromosome Location	chr3:134537692-134537693
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1399704	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1399705	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1808118	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34642200	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34848452	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35273483	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35843718	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59885053	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs71331778	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877515	chr3:134460368-134591138	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134529600-134541800	Weak transcription	Fetal Brain Female	brain
2	chr3:134529600-134542600	Weak transcription	Brain Germinal Matrix	brain
3	chr3:134529600-134546400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:134530000-134540800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr3:134530800-134541000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:134531200-134537800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:134534800-134546000	Weak transcription	Right Atrium	heart
8	chr3:134535800-134540800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr3:134537000-134541000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:134537000-134543000	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr3:134537000-134543400	Weak transcription	Psoas Muscle	Psoas
12	chr3:134537400-134537800	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr3:134537600-134537800	Enhancers	GM12878-XiMat	blood

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Input of quick search could be:

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

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