Variant report

Variant	rs2280608
Chromosome Location	chr7:78641410-78641411
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHTF2-3	chr7:78641400-78641593	ENSG00000226978.1

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1006818	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10215372	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10226001	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10236354	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10269689	0.89[EUR][1000 genomes]
rs10808175	0.95[EUR][1000 genomes]
rs11769552	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12113491	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12534480	0.88[EUR][1000 genomes]
rs12536821	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12536843	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12538053	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12669763	0.95[EUR][1000 genomes]
rs12705911	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1476106	0.95[EUR][1000 genomes]
rs2006635	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2079955	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2079956	0.81[ASN][1000 genomes]
rs2098180	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2098181	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2109713	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2191724	0.86[EUR][1000 genomes]
rs2191726	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2191727	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2191728	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2280607	0.97[ASN][1000 genomes]
rs2363930	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2363931	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs28572181	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs28716458	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs34086589	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4727794	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4727796	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4730596	0.95[EUR][1000 genomes]
rs4730597	0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4730599	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4730601	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4730619	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6466468	0.95[EUR][1000 genomes]
rs6466471	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6466477	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6952133	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs727652	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7779315	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7781812	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7789063	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7791770	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7792974	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7793390	0.89[EUR][1000 genomes]
rs7795421	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7797398	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799032	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7805367	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7807319	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7809089	0.90[EUR][1000 genomes]
rs9656215	0.89[EUR][1000 genomes]
rs984312	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv482826	chr7:78548319-78717605	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv471642	chr7:78548320-78717605	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1029799	chr7:78608097-79061737	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv831040	chr7:78623195-78831998	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv521257	chr7:78632489-78662425	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr7:78632600-78648800	Weak transcription	Aorta	Aorta

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