Variant report

Variant	rs6543613
Chromosome Location	chr2:31402079-31402080
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10168043	0.82[AMR][1000 genomes]
rs10180369	0.82[AMR][1000 genomes]
rs10184618	0.80[AMR][1000 genomes]
rs10192576	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10445909	0.81[AMR][1000 genomes]
rs12105593	0.81[AMR][1000 genomes]
rs13387367	0.81[AMR][1000 genomes]
rs13387507	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13389654	0.82[AMR][1000 genomes]
rs13389667	0.82[AMR][1000 genomes]
rs13409609	0.82[AMR][1000 genomes]
rs13421448	0.81[AMR][1000 genomes]
rs13421721	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13423585	0.81[AMR][1000 genomes]
rs1443706	0.82[AMR][1000 genomes]
rs1443707	0.82[AMR][1000 genomes]
rs2028675	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2028676	0.84[AMR][1000 genomes]
rs2028677	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2028678	0.84[AMR][1000 genomes]
rs28684727	0.81[AMR][1000 genomes]
rs4516476	0.82[AMR][1000 genomes]
rs4592896	0.82[AMR][1000 genomes]
rs57684646	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs59788807	0.81[AMR][1000 genomes]
rs60854003	0.84[AMR][1000 genomes]
rs6543611	0.82[AMR][1000 genomes]
rs6715931	0.82[AMR][1000 genomes]
rs6716920	0.81[AMR][1000 genomes]
rs6720151	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6720254	0.82[AMR][1000 genomes]
rs7556787	0.82[AMR][1000 genomes]
rs7564370	0.83[AMR][1000 genomes]
rs7564478	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7567330	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7567449	0.83[AMR][1000 genomes]
rs7570373	0.81[AMR][1000 genomes]
rs7578398	0.83[AMR][1000 genomes]
rs7579175	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7593899	0.83[AMR][1000 genomes]
rs7602639	0.82[AMR][1000 genomes]
rs9308918	0.81[AMR][1000 genomes]
rs9753207	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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	9 gene(s)	inside rSNPs	diseases
2	nsv873771	chr2:31363732-31416582	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv873772	chr2:31363732-31417863	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv873773	chr2:31363732-31426449	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv873774	chr2:31363732-31432367	Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv873775	chr2:31363732-31439443	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv873776	chr2:31384009-31439443	Enhancers Bivalent Enhancer Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv997652	chr2:31385242-31431588	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv535611	chr2:31385242-31431588	ZNF genes & repeats Strong transcription Enhancers Weak transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 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	chr2:31388400-31407000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr2:31391200-31418600	Weak transcription	Gastric	stomach
3	chr2:31394800-31419600	Weak transcription	Primary B cells from cord blood	blood
4	chr2:31395200-31416600	Weak transcription	Primary B cells from peripheral blood	blood
5	chr2:31395800-31415000	Weak transcription	Esophagus	oesophagus

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