Variant report

Variant	rs13326802
Chromosome Location	chr3:142689347-142689348
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs1392177	0.88[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1392179	0.80[AFR][1000 genomes]
rs2069250	0.90[AMR][1000 genomes]
rs2276758	0.90[AMR][1000 genomes]
rs251493	0.90[ASN][1000 genomes]
rs251494	0.91[ASN][1000 genomes]
rs36286	0.93[ASN][1000 genomes]
rs3732743	0.88[AMR][1000 genomes]
rs58904989	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs73003373	0.80[AFR][1000 genomes]
rs73866285	0.83[ASN][1000 genomes]
rs9844683	0.93[AMR][1000 genomes];0.82[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	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:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142683600-142691800	Weak transcription	A549	lung
2	chr3:142684400-142691200	Weak transcription	Liver	Liver
3	chr3:142684800-142689800	Enhancers	K562	blood
4	chr3:142688200-142690800	Weak transcription	Fetal Heart	heart
5	chr3:142688600-142691600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:142689200-142689400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:142689200-142689400	Bivalent Enhancer	HepG2	liver

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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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