Variant report

Variant	rs58526779
Chromosome Location	chr7:147697602-147697603
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10226093	0.90[EUR][1000 genomes]
rs10227836	0.82[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10236799	0.90[EUR][1000 genomes]
rs10241081	0.90[EUR][1000 genomes]
rs10250801	0.90[EUR][1000 genomes]
rs10257780	0.81[EUR][1000 genomes]
rs10261595	0.92[AFR][1000 genomes]
rs10261693	0.92[AFR][1000 genomes]
rs10270437	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10270778	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs10273095	0.81[EUR][1000 genomes]
rs10273493	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10276274	0.81[EUR][1000 genomes]
rs10276996	0.92[AFR][1000 genomes]
rs10279557	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11972972	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11974390	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11976838	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11979926	0.84[AFR][1000 genomes]
rs12539425	0.95[AFR][1000 genomes]
rs28373395	0.86[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs28377968	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs28394241	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs28554472	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs28594409	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs28693625	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs34024797	0.95[AFR][1000 genomes]
rs57055307	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs58083908	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs58092267	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs58848818	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs60119393	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs60692572	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6970931	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs719311	0.95[AFR][1000 genomes]
rs73464297	0.87[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs73466110	0.94[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs73466115	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73466190	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs73466195	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs73468119	0.90[EUR][1000 genomes]
rs73468120	0.90[EUR][1000 genomes]
rs7780623	0.93[AFR][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	nsv1023913	chr7:147521075-147806318	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	6 gene(s)	inside rSNPs	diseases
2	nsv1026058	chr7:147521109-147783042	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv539179	chr7:147521109-147783042	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv934002	chr7:147521110-147807705	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1017610	chr7:147523752-147806427	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv889399	chr7:147643923-147712471	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv889400	chr7:147650411-147712471	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147696600-147697800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr7:147696600-147698200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr7:147696800-147698000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr7:147696800-147698000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr7:147697000-147698200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr7:147697200-147698000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr7:147697200-147698200	Enhancers	H1 Cell Line	embryonic stem cell
8	chr7:147697400-147697800	Enhancers	HUES64 Cell Line	embryonic stem cell

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