Variant report

Variant	rs7789308
Chromosome Location	chr7:64301535-64301536
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10236712	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10236731	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10251093	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10251096	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10255015	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10255285	1.00[AMR][1000 genomes]
rs10266341	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10266823	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10266953	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10267569	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10267592	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10275714	1.00[ASW][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10278712	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10282236	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11978309	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12155450	1.00[AMR][1000 genomes]
rs12671429	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13237903	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13247714	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs1464925	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1464926	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1525811	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs1568913	0.80[AFR][1000 genomes]
rs1608896	1.00[YRI][hapmap]
rs1815165	0.94[AFR][1000 genomes]
rs1815168	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1852205	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1852206	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1976918	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2015938	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2418462	1.00[ASW][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2418463	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2418464	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3983288	0.91[AFR][1000 genomes]
rs3983289	0.97[AFR][1000 genomes]
rs4236203	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4327747	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4327748	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4429995	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4483043	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4579410	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4613867	0.83[AFR][1000 genomes]
rs4639394	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4717214	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4717215	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4717218	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718117	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718118	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718119	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718120	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718121	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718126	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718128	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718130	1.00[YRI][hapmap]
rs4718132	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718133	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718134	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718136	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4718137	0.97[AFR][1000 genomes]
rs55960866	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6460187	1.00[AMR][1000 genomes]
rs6460188	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6460190	1.00[AMR][1000 genomes]
rs6460191	0.94[AFR][1000 genomes]
rs6460193	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6460194	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6942695	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6943322	1.00[AMR][1000 genomes]
rs6943573	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6951133	1.00[AMR][1000 genomes]
rs6951316	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6953310	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6956506	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6957671	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6964400	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6965217	1.00[AMR][1000 genomes]
rs6971507	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6976049	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6976060	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7784682	1.00[MEX][hapmap]
rs7785568	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7790245	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7790631	1.00[MEX][hapmap]
rs7791652	0.97[AFR][1000 genomes]
rs7791673	0.80[AFR][1000 genomes]
rs7791951	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7799440	0.92[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7808059	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7809431	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7810921	1.00[AMR][1000 genomes]
rs9654821	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9654823	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9654824	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9718984	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422405	chr7:63709739-64632341	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv427787	chr7:63741770-64419520	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv2755057	chr7:63819849-64345822	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
4	nsv464518	chr7:63881238-64506904	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv607312	chr7:63881238-64506904	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv888274	chr7:63990100-64331123	Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
7	nsv888275	chr7:63990100-64468590	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv888276	chr7:63990100-64511564	Strong transcription ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv888279	chr7:64094285-64331123	Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
10	nsv1022042	chr7:64226499-64566945	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1026390	chr7:64240323-64414364	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv1033291	chr7:64273434-64406276	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv508457	chr7:64286522-64391112	Strong transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
14	esv1797468	chr7:64296309-64356050	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv888282	chr7:64299645-64511564	Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64300200-64301800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr7:64300200-64310000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:64301000-64302000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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