Variant report

Variant	rs74042393
Chromosome Location	chr13:30294883-30294884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs12854608	0.94[ASN][1000 genomes]
rs1571255	0.89[EUR][1000 genomes]
rs1747058	0.89[EUR][1000 genomes]
rs1747059	0.89[EUR][1000 genomes]
rs2182778	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2794296	0.89[EUR][1000 genomes]
rs2794299	0.89[EUR][1000 genomes]
rs3118078	0.89[EUR][1000 genomes]
rs34730463	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4083609	0.89[EUR][1000 genomes]
rs4142339	0.89[EUR][1000 genomes]
rs4142340	0.89[EUR][1000 genomes]
rs4399408	0.89[EUR][1000 genomes]
rs4580011	0.94[ASN][1000 genomes]
rs4769773	0.89[EUR][1000 genomes]
rs59768871	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61424636	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6490427	0.89[EUR][1000 genomes]
rs6490428	0.89[EUR][1000 genomes]
rs7322158	0.89[EUR][1000 genomes]
rs73444211	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73444214	0.94[ASN][1000 genomes]
rs74042382	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74042383	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74042387	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74042388	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74042389	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74042390	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74042392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74044752	0.89[EUR][1000 genomes]
rs7983788	0.89[EUR][1000 genomes]
rs8001320	0.89[EUR][1000 genomes]
rs912394	0.89[EUR][1000 genomes]
rs9508551	0.89[EUR][1000 genomes]
rs9550492	0.89[EUR][1000 genomes]
rs9551729	0.88[ASN][1000 genomes]
rs9579469	0.94[ASN][1000 genomes]
rs9579472	0.94[ASN][1000 genomes]
rs9788356	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899961	chr13:30226924-30407273	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	esv3520592	chr13:30243601-30648554	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	esv3520593	chr13:30243601-30648554	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:30292200-30295000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr13:30294200-30295200	Weak transcription	Spleen	Spleen
3	chr13:30294200-30296000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr13:30294400-30295000	Enhancers	Primary neutrophils fromperipheralblood	blood

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