Variant report

Variant	rs73489137
Chromosome Location	chr7:119482774-119482775
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:119481189..119482862-chr7:119504225..119505878,2	K562	blood:
2	chr7:119482560..119485334-chr7:119486434..119488140,2	K562	blood:

Extended variants
information (count: 90 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10085666	1.00[ASN][1000 genomes]
rs10281584	1.00[ASN][1000 genomes]
rs12333906	1.00[ASN][1000 genomes]
rs12374758	1.00[ASN][1000 genomes]
rs12533333	1.00[ASN][1000 genomes]
rs1533983	1.00[ASN][1000 genomes]
rs1581503	1.00[ASN][1000 genomes]
rs17142322	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17142348	1.00[ASN][1000 genomes]
rs17142414	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1916858	1.00[ASN][1000 genomes]
rs2140567	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2140568	1.00[ASN][1000 genomes]
rs2204310	1.00[ASN][1000 genomes]
rs2402487	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs28549838	0.82[AMR][1000 genomes]
rs28600065	0.82[AMR][1000 genomes]
rs28760947	1.00[ASN][1000 genomes]
rs28776558	1.00[ASN][1000 genomes]
rs4449718	1.00[ASN][1000 genomes]
rs4493836	1.00[ASN][1000 genomes]
rs4610676	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs56291644	1.00[ASN][1000 genomes]
rs58473239	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58538319	1.00[ASN][1000 genomes]
rs60495904	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60744696	1.00[ASN][1000 genomes]
rs61081273	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6944434	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6945733	1.00[ASN][1000 genomes]
rs6947563	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6952445	1.00[ASN][1000 genomes]
rs6954234	1.00[ASN][1000 genomes]
rs6964883	1.00[ASN][1000 genomes]
rs6964884	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6975903	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73472908	1.00[ASN][1000 genomes]
rs73472910	1.00[ASN][1000 genomes]
rs73485196	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs73485199	0.82[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs73485200	1.00[ASN][1000 genomes]
rs73487136	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487146	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487152	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487156	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487158	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs73487167	0.97[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487175	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487178	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487179	1.00[ASN][1000 genomes]
rs73487183	1.00[ASN][1000 genomes]
rs73487186	1.00[ASN][1000 genomes]
rs73487191	1.00[ASN][1000 genomes]
rs73487193	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487195	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73487201	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73489103	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73489107	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73489110	1.00[ASN][1000 genomes]
rs73489120	1.00[ASN][1000 genomes]
rs73489138	1.00[ASN][1000 genomes]
rs73489140	1.00[ASN][1000 genomes]
rs73489143	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73489150	1.00[ASN][1000 genomes]
rs73489153	1.00[ASN][1000 genomes]
rs73722666	1.00[ASN][1000 genomes]
rs7780733	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7797664	1.00[ASN][1000 genomes]
rs7799517	1.00[ASN][1000 genomes]
rs7809848	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs846433	1.00[ASN][1000 genomes]
rs846435	1.00[ASN][1000 genomes]
rs846449	1.00[ASN][1000 genomes]
rs882837	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs884489	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9690438	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889115	chr7:119270386-119577292	ZNF genes & repeats Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1029023	chr7:119292763-119606632	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1023813	chr7:119292763-119606803	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv524225	chr7:119293417-119606632	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1029841	chr7:119299627-119606632	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1024175	chr7:119299627-119606803	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1018500	chr7:119310497-119532489	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1028812	chr7:119310497-119604904	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv539097	chr7:119310497-119604904	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1033418	chr7:119324894-119600025	Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv539098	chr7:119324894-119600025	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1018731	chr7:119411352-119493951	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	nsv1025273	chr7:119412165-119493951	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv470388	chr7:119464310-119790102	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119481600-119485000	Strong transcription	K562	blood
2	chr7:119482400-119483400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr7:119482600-119483000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr7:119482600-119483400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr7:119482600-119483400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr7:119482600-119483600	Enhancers	H9 Cell Line	embryonic stem cell
7	chr7:119482600-119483600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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