Variant report

Variant	rs2447834
Chromosome Location	chr5:103912354-103912355
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs1443071	0.83[AMR][1000 genomes]
rs168829	0.84[EUR][1000 genomes]
rs17156785	0.83[AMR][1000 genomes]
rs2431106	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2431107	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2431113	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2439978	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2447830	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2447835	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2447836	0.95[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2447837	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2455315	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs254009	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs254010	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs254036	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs33816	0.83[EUR][1000 genomes]
rs375770	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs387973	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs394755	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs401327	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs409647	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs411152	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs419682	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs424906	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs454662	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6596580	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6596581	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6596582	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6596583	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7722572	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882524	chr5:103237745-104019292	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv531969	chr5:103482070-104249804	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv432793	chr5:103693025-104115101	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv428121	chr5:103777677-104094645	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1022638	chr5:103789145-104682389	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv882537	chr5:103833944-103925210	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv830433	chr5:103862974-103983492	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv462337	chr5:103906144-103971846	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv471029	chr5:103906144-103971846	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv599215	chr5:103906144-103971846	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:103912000-103912800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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