Variant report

Variant	rs1392177
Chromosome Location	chr3:142684597-142684598
allele	A/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:9)

rs_ID	r²[population]
rs13326802	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2069250	0.97[AMR][1000 genomes]
rs2276758	0.97[AMR][1000 genomes]
rs251493	0.90[ASN][1000 genomes]
rs251494	0.92[ASN][1000 genomes]
rs36286	0.90[ASN][1000 genomes]
rs3732743	0.95[AMR][1000 genomes]
rs58904989	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9844683	0.86[AMR][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	nsv877562	chr3:142573789-142846370	Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv877563	chr3:142661350-142743889	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142683400-142684800	Weak transcription	K562	blood
2	chr3:142683400-142687200	Weak transcription	Left Ventricle	heart
3	chr3:142683600-142691800	Weak transcription	A549	lung
4	chr3:142684400-142684600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
5	chr3:142684400-142691200	Weak transcription	Liver	Liver

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

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