Variant report

Variant	rs67618266
Chromosome Location	chr7:47739673-47739674
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10224672	0.85[AMR][1000 genomes]
rs10226887	0.85[AMR][1000 genomes]
rs10227002	0.85[AMR][1000 genomes]
rs10227130	0.85[AMR][1000 genomes]
rs10227440	0.94[ASN][1000 genomes]
rs10227920	0.94[ASN][1000 genomes]
rs10240563	0.95[ASN][1000 genomes]
rs10242348	0.86[AMR][1000 genomes]
rs10245141	0.94[ASN][1000 genomes]
rs10245264	0.94[ASN][1000 genomes]
rs10253662	0.92[ASN][1000 genomes]
rs10255901	0.85[AMR][1000 genomes]
rs10256144	0.85[AMR][1000 genomes]
rs10256699	0.89[ASN][1000 genomes]
rs10257547	0.94[ASN][1000 genomes]
rs10266879	0.85[AMR][1000 genomes]
rs10266971	0.85[AMR][1000 genomes]
rs10272181	0.85[AMR][1000 genomes]
rs10274400	0.94[ASN][1000 genomes]
rs10275398	0.85[AMR][1000 genomes]
rs10275720	0.85[AMR][1000 genomes]
rs10275779	0.80[AMR][1000 genomes]
rs10275780	0.80[AMR][1000 genomes]
rs10280669	0.80[ASN][1000 genomes]
rs11760321	0.83[AMR][1000 genomes]
rs11762285	0.85[AMR][1000 genomes]
rs11763432	0.85[AMR][1000 genomes]
rs11764002	0.96[ASN][1000 genomes]
rs11764105	0.95[ASN][1000 genomes]
rs11766220	0.85[AMR][1000 genomes]
rs11767556	0.96[ASN][1000 genomes]
rs11770388	0.83[AMR][1000 genomes]
rs11772165	0.88[AMR][1000 genomes]
rs11772364	0.85[AMR][1000 genomes]
rs11772424	0.85[AMR][1000 genomes]
rs11773187	0.85[AMR][1000 genomes]
rs11773422	0.85[AMR][1000 genomes]
rs28712803	0.94[ASN][1000 genomes]
rs28766091	0.94[ASN][1000 genomes]
rs28795431	0.94[ASN][1000 genomes]
rs28869205	0.94[ASN][1000 genomes]
rs28886403	0.93[ASN][1000 genomes]
rs28893025	0.94[ASN][1000 genomes]
rs4720606	0.83[AMR][1000 genomes]
rs4720607	0.85[AMR][1000 genomes]
rs4720609	0.85[AMR][1000 genomes]
rs4720610	0.85[AMR][1000 genomes]
rs4720611	0.83[AMR][1000 genomes]
rs4720612	0.83[AMR][1000 genomes]
rs4724611	0.85[AMR][1000 genomes]
rs4724612	0.85[AMR][1000 genomes]
rs66674577	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs66780336	0.96[ASN][1000 genomes]
rs66931702	0.96[ASN][1000 genomes]
rs66979603	0.96[ASN][1000 genomes]
rs67043063	0.81[ASN][1000 genomes]
rs67344873	0.96[ASN][1000 genomes]
rs67853780	0.96[ASN][1000 genomes]
rs6956809	0.94[ASN][1000 genomes]
rs6956821	0.93[ASN][1000 genomes]
rs6970135	0.94[ASN][1000 genomes]
rs6974376	0.94[ASN][1000 genomes]
rs6974724	0.94[ASN][1000 genomes]
rs6975025	0.94[ASN][1000 genomes]
rs73107254	0.85[AMR][1000 genomes]
rs73107273	0.96[ASN][1000 genomes]
rs73107278	0.94[ASN][1000 genomes]
rs73109586	0.89[ASN][1000 genomes]
rs7776882	0.85[AMR][1000 genomes]
rs7791862	0.94[ASN][1000 genomes]
rs7792137	0.81[ASN][1000 genomes]
rs7792409	0.94[ASN][1000 genomes]
rs7792432	0.94[ASN][1000 genomes]
rs7792551	0.94[ASN][1000 genomes]
rs7792952	0.94[ASN][1000 genomes]
rs7793995	0.85[AMR][1000 genomes]
rs7794051	0.82[AMR][1000 genomes]
rs7794346	0.85[AMR][1000 genomes]
rs7804238	0.83[AMR][1000 genomes]
rs7811157	0.94[ASN][1000 genomes]
rs7811870	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026223	chr7:47560728-48243287	Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv888003	chr7:47694270-47907214	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1024392	chr7:47707023-47758976	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1018608	chr7:47708525-47831535	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv1024027	chr7:47709936-47743485	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1022906	chr7:47709936-47831535	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
7	nsv1028355	chr7:47715107-47758976	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1015163	chr7:47734913-47832389	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
9	nsv538831	chr7:47734913-47832389	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
10	esv3427240	chr7:47737127-47741925	Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	esv3388027	chr7:47738477-47741275	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:47731200-47741600	Weak transcription	Right Atrium	heart
2	chr7:47733000-47750000	Weak transcription	Aorta	Aorta
3	chr7:47733200-47741400	Weak transcription	A549	lung
4	chr7:47734000-47748600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr7:47734600-47748200	Weak transcription	Fetal Stomach	stomach
6	chr7:47738400-47741600	Weak transcription	HSMMtube	muscle
7	chr7:47739400-47740000	ZNF genes & repeats	Fetal Kidney	kidney
8	chr7:47739600-47740000	Enhancers	Pancreas	Pancrea

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