Variant report

Variant	rs770385
Chromosome Location	chr13:51142969-51142970
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1239681	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1239682	0.86[EUR][1000 genomes]
rs1239683	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239684	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239686	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239687	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239688	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239689	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239690	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239691	0.85[EUR][1000 genomes]
rs1239692	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239693	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239695	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1239696	0.84[EUR][1000 genomes]
rs1239702	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1239703	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1239705	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239706	0.86[ASN][1000 genomes]
rs1239707	0.86[ASN][1000 genomes]
rs1270717	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1271766	0.85[EUR][1000 genomes]
rs2794469	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs706601	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs706602	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770383	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770384	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770386	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs770388	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770391	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770392	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770393	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs770394	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs770395	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs770396	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs947380	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs947382	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs947383	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9596313	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs978332	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	esv2753864	chr13:51136699-51375199	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr13:51142200-51146400	Weak transcription	Fetal Lung	lung

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